`Party
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`Correspondence
`Address
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`Submission
`Filer's Name
`Filer's e-mail
`Signature
`Date
`Attachments
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`Trademark Trial and Appeal Board Electronic Filing System. http://estta.uspto.gov
`ESTTA648481
`ESTTA Tracking number:
`01/06/2015
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`Filing date:
`IN THE UNITED STATES PATENT AND TRADEMARK OFFICE
`BEFORE THE TRADEMARK TRIAL AND APPEAL BOARD
`92054171
`Defendant
`VGO Communications, Inc.
`MICHAEL J BEVILACQUA
`WILMER CUTLER ET AL
`60 STATE ST
`BOSTON, MA 02109
`UNITED STATES
`Barbara.Barakat@wilmerhale.com, angela.dyer@wilmerhale.com, Mi-
`chael.Bevilaqua@wilmerhale.com
`Opposition/Response to Motion
`John V. Hobgood
`John.Hobgood@WilmerHale.com
`/John V. Hobgood/
`01/06/2015
`Filing_Correcting_Redaction.PDF(16771 bytes )
`Registrant's_Opposition_to_SJM_(REDACTED).PDF(138885 bytes )
`Exhibits_to_Opposition_to_SJM_(A_-_G).PDF(4329651 bytes )
`Exhibit_to_Opposition_to_SJM_(H).PDF(5149696 bytes )
`Exhibits_to_Opposition_to_SJM_(I_-_N)_(REDACTED).PDF(3328518 bytes )
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`IN THE UNITED STATES PATENT AND TRADEMARK OFFICE
`BEFORE THE TRADEMARK TRIAL AND APPEAL BOARD
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`Valeritas, Inc.,
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`Petitioner,
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`v.
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`VGo Communications, Inc.,
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`__________________________________________
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`Registrant.
`__________________________________________)
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`Cancellation No. 92054171
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`REGISTRANT’S CORRECTION OF INADVERTENT FILING OF PROTECTED
`MATERIALS
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`On December 15, 2014, Registrant VGo Communications, Inc. submitted its opposition
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`to Petitioner Valeritas, Inc.’s Motion for Summary Judgment. In its submission, Registrant
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`supplied a copy of Petitioner’s Second Supplemental Responses to Registrant’s Interrogatories in
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`Exhibit I that had been marked “Confidential – For Attorneys’ Eyes Only”. Registrant also
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`included a quote from the third page of Petitioner’s responses in Registrant’s memorandum.
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`Because the confidential designation did not appear on the third page, but was made only on the
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`first page of the responses, Registrant inadvertently did not redact this material.
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`Upon being made aware of the situation, counsel for Registrant contacted the Trademark
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`Trial and Appeal Board staff and had the inadvertent disclosure marked confidential, thereby
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`rendering it unavailable via TTABVue. In this filing, Registrant supplies a copy of its original
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`December 15, 2014, filing with the appropriate redactions in its memorandum and Exhibit I.
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`ActiveUS 139553351v.1
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`VGo Communications. Inc..
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`By its attorneys,
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` /John V. Hobgood/
`____________________________________
`Michael J. Bevilacqua
`Barbara A. Barakat
`John V. Hobgood
`Wilmer Cutler Pickering Hale and Dorr LLP
`60 State Street
`Boston, Massachusetts 02109
`(617) 526-6000
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`January 6, 2015
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`Certificate Of Service
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`I certify that a true copy of the foregoing Registrant’s Correction of Inadvertent Filing of
`Protected Materials and redacted copy of its December 15, 2014, filing is being served by first-
`class mail, postage-prepaid, this 6th day of January, 2015, upon:
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`Sheri S. Mason, Esq.
`Thomas F. Dunn, Esq.
`Morse, Barnes-Brown & Pendleton, P.C.
`CityPoint
`230 Third Avenue, 4th Floor
`Waltham, Massachusetts 02451
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`Date of Deposit:
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`1/6/2015
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`Signature:
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` /John V. Hobgood/ .
` John V. Hobgood
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`IN THE UNITED STATES PATENT AND TRADEMARK OFFICE
`BEFORE THE TRADEMARK TRIAL AND APPEAL BOARD
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`Valeritas, Inc.,
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`Petitioner,
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`v.
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`VGo Communications, Inc.,
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`__________________________________________
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`Registrant.
`__________________________________________)
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`Cancellation No. 92054171
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`REGISTRANT’S OPPOSITION TO PETITIONER’S MOTION FOR SUMMARY
`JUDGMENT AND MEMORANDUM IN SUPPORT THEREOF
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`
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`Registrant VGo Communications, Inc. respectfully submits its opposition to Petitioner
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`Valeritas, Inc.’s Motion for Summary Judgment, pursuant to Rule 2.116 of the Trademark Rules
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`of Practice, 37 C.F.R. §2.127(e) of the Federal Rules of Procedure.
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`I.
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`PROCEDURAL HISTORY
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`On March 2, 2010, Registrant filed an application to register its trademark VGO on the
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`basis of an intention to use the mark in commerce with the following goods, “robotic video and
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`audio communication hardware; computer software for use in connection with audio and video
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`communication systems.” A registration was issued from this application on December 21,
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`2010. Petitioner filed its Petition for Cancellation on June 28, 2011. The parties exchanged
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`Initial Disclosures in October 2011 and conducted discovery from November 2011 through
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`November 2014. During the discovery period, the parties attempted on numerous occasions to
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`settle the matter but were unable to reach agreement. Petitioner served its Motion for Summary
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`Judgment on November 8, 2014.
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`Registrant now responds to Petitioner’s Motion for Summary Judgment.
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`II. ARGUMENT
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`A. The Standard for Summary Judgment
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`Rule 56(a) of the Federal Rules of Civil Procedure, adopted as TBMP §528, allows for
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`summary judgment when there are no genuine issues of material fact in dispute. Summary
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`judgment is inappropriate if a dispute about a material fact is genuine, “that is, if the evidence is
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`such that a reasonable jury could return a verdict for the nonmoving party.” Anderson v. Liberty
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`Lobby, Inc., 477 U.S. 242, 248 (1986). Summary judgment will be granted “only where the
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`moving party is entitled to judgment as a matter of law, where it is quite clear what the truth is, .
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`. . [and where] no genuine issue remains for trial . . . [for] the purpose of the rule is not to cut
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`litigants off from the right of trial . . . if they really have issues to try.” Poller v. Columbia
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`Broadcasting Sys., Inc., 368 U.S. 464,467 (1962) (quoting Sartor v. Arkansas Natural Gas Corp.,
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`321 U.S. 620, 627 (1944)).
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`To prevail on its Motion, Petitioner must prove that there are no disputed facts and that
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`there is an “absence of evidence to support the non-moving party’s case.” TBMP §528.01. “The
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`burden in a motion for summary judgment is on the moving party to establish prima facie that
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`there is no genuine issue of material fact . . .” Shalom Children’s Wear Inc. v. ln-Wear A/S, 26
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`USPQ2d 1516, 1518 (TTAB 1993), and “all inferences to be drawn from the undisputed facts
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`must be viewed in the light most favorable to the nonmoving party. . .” Moreover, “[a]ll doubts
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`as to whether or not particular factual issues are genuinely in dispute must be resolved against
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`the moving party.” Flately v. Trump, 11 USPQ2d 1284, 1287 (TTAB 1989).
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`When all inferences are drawn in favor of Registrant VGo Communications, Inc., this
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`Cancellation presents genuine issues of material fact which compel denial of Petitioner Valeritas,
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`Inc.’s Motion for Summary Judgment.
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`B. Statement of Disputed Factual Issue
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`The following unresolved issue of material fact precludes Summary Judgment: Whether
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`there is a likelihood of confusion in view of the differences between the marks, the differences in
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`the goods upon which the marks are used, the channels of trade in which the marks will be
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`marketed and sold, the sophistication of the consumers, the lack of any actual confusion, and
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`other factors distinguishing the marks.
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`C. The Marks are not likely to be confused
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`An examination of the factors set forth in In re E.I. DuPont DeNemours & Co., 476 F.2d
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`1357 (CCPA 1973), reveals numerous unresolved issues of material fact, precluding Summary
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`Judgment in Petitioner’s favor. Indeed, a cursory review of the record indicates that the majority
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`of the factors overall support Registrant’s contention that confusion is unlikely.
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`1. The Marks Differ in Appearance and Commercial Impression.
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`Petitioner argues that the similarities in its mark and Registrant’s mark in standard
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`characters make the marks virtually identical. Petitioner suggests that this alone requires the
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`Board to determine that the parties marks are confusingly similar. See Petitioner’s Motion for
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`Summary Judgment at pg. 7. However, as set forth in more detail below, significant differences
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`in other factors relevant to likelihood of confusion show unresolved genuine issues of material
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`facts that render summary judgment inappropriate and, in fact, compel a determination that
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`confusion is unlikely.
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`Petitioner compares the mark from Registrant’s specimen of use filed with its application
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`(Registrant’s Design Mark) to Petitioner’s Mark Reg. No. 4,105,936 (Petitioner’s Design Mark),
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`but Petitioner ignores material differences in appearance, connotation, and commercial
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`impression between the marks1. Petitioner’s Certificate of Registration, showing its Design
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`Mark, and Registrant’s specimen of use, showing its Design Mark, are set forth below and are
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`also provided in Exhibits A, and B, respectively.
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`As shown above, Petitioner’s Design Mark includes the words “DISPOSABLE INSULIN
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`DELIVERY” in dark green below the “GO” component of the mark. Meanwhile, Registrant’s
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`Design Mark has no other letter or word components aside from the letters “VGO” comprising
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`the majority of the mark. The marks differ significantly in color scheme; the letters “VGO” of
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`Registrant’s Design Mark are a single color, while those of Petitioner’s Design Mark are two-
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`tone with the “V” in dark green and the “GO” in lime green. The font and letter layout of the
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`marks differ as well. The letters “G” and “O” of Registrant’s Design Mark have a rounded
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`square shape, the “G” overlaps with the “V”, and the letters “GO” fall roughly in the middle of
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`the “V” from a vertical standpoint. The letters “G” and “O” of Petitioner’s Design Mark have a
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`1 Petitioner cites Phillips Petroleum Company v. C.J. Webb, Inc., 170 U.S.P.Q. 35 (C.C.P.A. 1971) to support its
`comparison of its Design Mark to Registrant’s specimen of record. Petitioner discusses only the portion of Phillips
`in which that court found a high degree of similarity between the opposer’s and applicant’s marks and states, “As a
`result the court found a likelihood of confusion and reversed the TTAB’s decision dismissing the opposition.” See
`Petitioner’s Motion of Summary Judgment at pgs. 4-5. However, the Phillips Court did not decide likelihood of
`confusion based on a similarity of the marks alone. That court also found that Phillips’s mark was old and well
`known for petroleum products (dating back to Nov. 22, 1949) and that applicant’s and Phillips’s products were
`sufficiently similar. These later two factors are absent in the present cancellation, as is a sufficient similarity of the
`marks.
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`circular shape, there is no overlap between the letters, and the letters “GO” are top justified with
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`the letter “V”.
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`Registrant’s Design Mark has a wheel symbol comprised of two arcs trailed by two
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`pointed lines, which underline all three letters “VGO”. Petitioner has no such underline, but
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`instead points to a hyphen that crosses the word “GO” to find a similarity between the marks.
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`Petitioner states that Registrant’s rolling wheel element and Petitioner’s hyphen element suggest
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`movement from left to right. However, in its Registration, Petitioner states, “The hyphen is a
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`stylized design intended to represent a finger prick used to drawing [sic] blood for testing.” See
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`Exhibit A. Moreover, when asked during her deposition what the hyphen element represented,
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`Ms. Tara Charvat, Vice President Marketing and Marketing Operations for Petitioner, answered,
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`“The needle button on the V-Go device.” See Deposition of Tara L. Charvat, attached as Exhibit
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`C at 78:1-4. Thus, Petitioner has suggested three different impressions this element alone would
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`make on the consumer. Which of these three impressions is appropriate, how that impression
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`contributes to the overall connotation and commercial impression of the entire mark, and how
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`that impression contrasts with the overall impression of Registrant’s Design Mark is, by itself,
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`but one unresolved issue of material fact. See J. Thomas McCarthy, 4 McCarthy on Trademarks
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`and Unfair Competition § 23:26 (“[T]he ‘psychological imagery evoked by the respective marks’
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`may overpower the respective similarities or difference in appearance and sound.”); see also
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`Lever Bros. Co. v. Babson Bros. Co., 197 F.2d 531 (C.C.P.A. 1952). That the other differences
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`between the design marks set forth above must be weighed with any similarities shows that the
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`dissimilarity of the marks in their entireties is a genuine issue of material fact that renders
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`summary judgment inappropriate.
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`Because of all these differences, Petitioner’s Design Mark and Registrant’s Design Mark
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`create substantially different overall appearances, connotations and commercial impressions. It
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`is clear that genuine issues of material facts exist which compel denial of Petitioner’s Motion for
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`Summary Judgment.
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`2.
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`The goods are distinct.
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`The Petitioner’s goods are listed as “medical apparatus, namely, infusion and injection
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`devices for administering drugs” in class 10. Petitioner’s Vice President of Marketing described
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`the product as “A disposable insulin delivery device,” that “delivers insulin over a 24-hour
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`period which you can take off and remove after that 24 hours and throw out.” See Exhibit C at
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`10:20-12:5. Petitioner’s Chief Executive Officer explains that its core product is designed for
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`Type 2 diabetics, and, in use, “You insert it with insulin and then the patient puts it on their
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`body, on the abdomen, and they click a couple of buttons and they deliver insulin on a
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`continuous 24-hour basis. And then they click other buttons which will deliver insulin at
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`mealtime.” See Deposition of Kristen Peterson, CEO of Petitioner, attached as Exhibit D at
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`13:13-19.
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`The Registrant’s goods are identified as “robotic video and audio communication
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`hardware; computer software for use in connection with audio and video communication
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`systems” in class 9. See Certificate of Registration No. 3,895,432, attached as Exhibit E. In the
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`Rule 30(b)(6) Deposition of VGo Communications, Inc., attached as Exhibit F, Registrant
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`describes its product as “a robotic telepresence system [that] is a robot with two-way audiovisual
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`communications.” See Exhibit F at 36:11-14. Registrant explained the meaning of “robotic
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`telepresence” as “a physical avatar … that has communication on a mobile platform that [one]
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`can control remotely … [One] can drive the robot and go and meet people and interact with
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`people remotely.” See id. at 36:15-37:2. In other words, Registrant’s goods are like a video
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`phone on wheels.
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`Registrant’s goods are not infusion and injection devices for administering drugs and are
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`not medical apparatus and, thus, do not fall within the range of the goods identified in the
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`Petitioner’s registration. Registrant’s goods are clearly not disposable insulin delivery devices
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`that continuously deliver insulin over a 24-hour period, and, indeed, do not deliver insulin or any
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`other drug in any form or manner. Moreover, Registrant’s goods do not treat or diagnose
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`diabetes or any other type of medical condition. Further still, Registrant’s products do not touch
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`a patient, do not in and of themselves monitor or assess a patient for diagnosis or treatment, and
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`do not administer any medication. Registrant’s product is a telepresence robot that provides two-
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`way audiovisual communications that enables its user to communicate (including by video
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`conference) with others remote from the user. It is difficult to believe that anyone would think
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`that a remote communication robot would deliver a continuous supply of insulin over a 24-hour
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`period or that such a robot and an insulin delivery device would be provided by the same source.
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`Illustrative images of Registrant’s and Petitioner’s goods in use follow below. The
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`source documents of these images are a Product Brochure describing Registrant’s products
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`(produced at VGO000001-002), attached as Exhibit G, and a Patient Instruction Manual for
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`Petitioner’s products (produced as VAL000672-698), attached as Exhibit H.
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`The picture on the left shows a user of Registrant’s telepresence robot participating in a
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`meeting with colleagues. The picture on the top right is a rendering of Petitioner’s disposable
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`insulin delivery device. The picture on the bottom right is a rendering of Petitioner’s product in
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`use by a patient.
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`Registrant’s telepresence robot is approximately 48 inches tall by 13 inches wide by 15
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`inches deep and weighs between 18-22 pounds. The telepresence robot has a motorized wheel
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`base that enables the user to move the robot from place-to-place as well as obstacle and stair
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`detection sensors to prevent collisions and damage while in motion. The robot also includes a
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`six inch LCD display, a camera, speakers, and a microphone array that enable its user to conduct
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`audio-video communications. See Exhibit G at VGO000002.
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`Petitioner’s disposable insulin delivery device is 2.4 inches long by 1.3 inches wide by
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`0.5 inches thick and weighs between 0.7-1.8 ounces. The insulin delivery device has an insulin
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`capacity reservoir between 0.56 – 0.76 mL. The device has an adhesive patch that holds the
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`device to the patient’s skin, e.g., the patient’s abdomen, as shown above. The device also
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`includes a needle that subcutaneously delivers insulin to the patient through the action of a
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`mechanically driven syringe. See Exhibit H at VGO000683, 000690.
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`Holding the evidence presented to date in the light most favorable to Registrant, there is a
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`question of material fact as to whether Registrant’s goods would be related to Petitioner’s goods
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`as they travel in commerce.
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`3.
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`There is no similarity between the Petitioner’s established, likely-to-continue
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`trade channels and Registrant’s established, likely-to-continue trade channels.
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`Petitioner’s product is used by individuals that have diabetes. See Exhibit D at 13:13-19.
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`Petitioner states that its product “
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`” See Petitioner’s Second Supplemental Responses to
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`Registrant’s Interrogatories, No. 16, attached as Exhibit I. Thus, Petitioner’s product must be
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`prescribed by a physician. See Exhibit C at 14:10-15. As a result, Petitioner sells its goods
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`“through all prescription based product channels.” See Petitioner’s Response to Registrant’s
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`First Set of Interrogatories, No. 6, attached as Exhibit J. Importantly, because the FDA requires
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`a prescription for Petitioner’s product, the individual end user of the product must consult a
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`health care professional before being able to obtain the product from a pharmacy of any kind.
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`Registrant’s product does not require a prescription – it is a telepresence robot – and does
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`not require an FDA-clearance. Thus, Registrant does not sell its products through pharmacies,
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`other prescription based product channels, or retail outlets. Rather, Registrant sells its goods
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`directly or through Value Added Resellers. See Registrant’s Responses to Petitioner’s First Set
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`of Interrogatories, No. 5, attached as Exhibit K. Moreover, Registrant seeks to “[provide] its
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`products to companies within the enterprise, education, and health care markets.” See id. at No.
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`4.
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`The Petitioner claims the parties’ products are closely related merely because Registrant
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`sells its products into the health care market. However, Registrant’s products are sold to the
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`enterprise and education markets as well. See Exhibit F at 42:12-15. Petitioner makes no claim
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`that it targets these later two markets. Although Petitioner ignores this issue, Petitioner’s own
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`exhibits to its Motion for Summary Judgment are replete with examples of Registrant’s
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`marketing efforts and the use of its products in the enterprise and education markets. See
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`Petitioner’s Motion for Summary Judgment, Exhibit I (VGO001327: schools use Registrant’s
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`products to enable home bound students to participate in class; VGO001329-1330: Registrant’s
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`products sold to Cisco, Intel, Ericsson, Massachusetts Institute of Technology, and Baylor
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`University; VGO001354: Automobile maker Audi uses Registrant’s products to enable technical
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`assistance consultants to remotely diagnose vehicle problems.)
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`Registrant markets and sells its products to the enterprise market, which includes, e.g.,
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`large enterprise, manufacturing, and small business consumers. Registrant’s products help its
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`enterprise consumers overcome distance, manage remote teams, and maintain a virtual presence
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`at many geographically distant locations at once. For example, Registrant’s products also enable
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`remote engineers and remote project team leaders to engage in processes and keep visually
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`involved in engineering, product development, and manufacturing projects. In another
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`illustrative application, Registrant’s products were used by a telecommunications company to
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`virtually attend the 2012 Consumer Electronics Show (CES). Registrant’s telepresence robot
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`enabled the company’s representative to interact with others in the company’s booth at CES as
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`well as move about the conference and interact with other vendors. See Registrant Solution
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`Examples, attached as Exhibit L.
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`Registrant also markets and sells its products to the educational market. Registrant’s
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`products enable students with disabilities and immune-deficiencies to attend classes virtually via
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`the products’ audio-video communication link to the telepresence robot. Students who are
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`unable to physically attend school due to their illness or condition are able to move between
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`classrooms independently and socialize with their friends via Registrant’s products. See
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`Registrant Solution Examples, attached as Exhibit M.
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`Moreover, in the health care market, Registrant does not specifically target individuals
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`for sale of its products, but rather targets “the chief information officer, the IT department, [or]
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`the chief innovation officer of heath care institutions.” See Exhibit F at 50:11-19; 60:14-19. To
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`the extent Registrant advertises to individual health care providers, e.g., individual physicians, it
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`does so to identify possible needs to those in IT departments. See Exhibit F at 92:2-94:7. In
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`other words, Registrant does not target the patient segment of the health care market, but rather
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`the information technology segment of the health care market. It is appropriate for the Board to
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`consider whom within the health care market makes the buying decisions when determining
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`whether a likelihood of confusion exists. In Astra Pharm. Prods., Inc. v. Beckman Instruments.,
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`Inc. 718 F.2d 1201 (1st Cir.1983), the court found no likelihood of confusion between two uses
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`of the identical mark “ASTRA”. In Astra, the plaintiff, appellant sold mainly local anesthetics,
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`cardiovascular medicines, and prefilled syringes. Id. at 1205. Meanwhile, the defendant,
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`appellee sold a computerized instrument that measured the quantities of various substances in a
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`patient’s blood. Id. at 1203-04.
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`The Astra court recognized that the products in question were all marketed to, sold to,
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`and used in hospitals. See Astra, 718 F.2d at 1206-07. However, the decision to purchase
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`appellant’s products was made through the hospital pharmacy, while the appellee’s blood
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`analyzer was marketed to the hospital chemistry lab. Id. at 1206. In recognizing this difference
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`as important to finding no likelihood of confusion, the court stated, “The ‘hospital community’ is
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`not a homogeneous whole, but is composed of separate departments with diverse purchasing
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`requirements, which, in effect, constitute different markets for the parties’ respective products.”
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`Id. at 1207.
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`
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`Because of the differences in the nature of the products, the manner in which they will
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`come to be used, the markets into which they are sold, and the market segments to which they
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`are marketed, it is clear that genuine issues of material facts as to the similarity of the channels of
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`trade for these products exist which compel denial of Petitioner’s Motion for Summary
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`Judgment.
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`4.
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`The Conditions under which and Buyers to whom sales are made prevent
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`confusion.
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`The goods of both the Petitioner and the Registrant are not impulse purchases. In the
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`case of the Petitioner, a consumer will have diabetes, the consumer must see a health care
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`professional to have it diagnosed, the health care profession will offer a prescription for the
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`treatment, and the consumer must then go to another party to purchase the goods for the
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`treatment. Indeed, an individual purchasing Petitioner’s product does so out of medical necessity
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`and not on a whim. Thus, necessarily, health care professionals are involved in the purchasing
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`decisions and dispensing of Petitioner’s goods. These health care professionals are sophisticated,
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`having necessarily been educated about the benefits, side effects, and dosages of drugs and drug
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`delivery systems. They are therefore likely to exercise more than the normal degree of care in
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`determining whether to prescribe the Petitioner’s products. See Astra, 718 F.2d at 1206-07
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`(health care provider “must be extremely cautious about what medicines it administers to its
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`patients, as well as their source.”). It goes without saying that a telepresence robot cannot be
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`used in place of an insulin delivery device for the treatment of diabetes. As a result, a health care
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`professional would not believe there is any connection between Petitioner’s and Registrant’s
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`products. Therefore, the required involvement of an educated health care professional assisting
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`in the selection of Petitioner’s products and educating the consumer about use of the products
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`ensures that there will be no likelihood of confusion.
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`Although for different reasons, consumers of Registrant’s products also carefully
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`consider the purchase of Registrant’s products. First, these consumers will most often be a
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`company, school, health care institution, or other large entity rather than an individual. Second,
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`the purchasing decision will be made by the chief information officer, member of the
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`information technology department, or member of the videoconferencing department of the
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`company, institution, or school. See Exhibit F at 42:12-15; 50:11-19; 60:14-19. Third, the cost
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`of Registrant’s products is $6,000-$7,000 for a single telepresence robot. See id. at 38:15-23.
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`Thus, the consumers of Registrant’s products will be sophisticated buyers purchasing relatively
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`expensive products, which ensures that there will be no likelihood of confusion. See Astra, 718
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`F.2d at 1206 (“[T]here is always less likelihood of confusion where goods are expensive and
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`purchased after careful consideration.”).
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`Because of the differences in the conditions under which sales are made, the differences
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`in the buyers to whom the sales are made, and the relatively high degree of care exercised in the
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`buying process, it is clear that genuine issues of material facts exist which compel denial of
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`Petitioner’s Motion for Summary Judgment.
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`5.
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`The record lacks evidence of actual confusion.
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`Petitioner first used its Design Mark in commerce on January 3, 2012. Meanwhile,
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`Registrant has continuously used its Design Mark in commerce since July 29, 2010. Registrant
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`is not aware of any instances of actual confusion between Registrant and/ Registrant’s Design
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`Mark on the one hand and Petitioner and/or Petitioner’s Design Mark on the other hand. See
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`Exhibit K at No. 3. Nor is Registrant aware of any instance in which any person has claimed to
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`be deceived, mistaken, or confused regarding the source of Registrant’s goods or services offered
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`under or in connection with Registrant’s Design Mark based on confusion with Petitioner and/or
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`Petitioner’s Design Mark. See id. at No. 8.
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`In its Responses to Registrant’s Interrogatories, Petitioner has identified only one
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`instance of what it claims to be actual confusion as to the identity of the parties herein or their
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`respective products or services.2 However, the evidence in the record concerning this lone
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`instance shows that the individual was not, in fact, confused as to the identity of the parties or
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`their products. Specifically, Petitioner states:
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`Dr. Richard E. Pratley notified Petitioner that he received
`information from [Registrant] referring to the V-GO mark. Dr.
`Pratley is Director of the Florida Hospital Diabetes Institute and
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`2 Registrant’s Interrogatory No. 8 of its First Set of Interrogatories states, “Describe each instance you know of
`wherein any person has been confused, mistaken or deceived as to the identity of the parties herein or their
`respective products or services.”
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`Senior Scientist and Professor at the Florida Hospital
`Sanford/Burnham Translational Research Institute. Dr. Pratley
`informed Petitioner, “Hey – somebody stole your name…..”
`See Exhibit J at No. 8.; Electronic mail from Dr. Richard Pratley, VAL000720-722, attached as
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`Exhibit N.
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`Holding the evidence of record in the light most favorable to Registrant, there is a
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`question of material fact as to whether Petitioner’s example shows an instance of actual
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`confusion. Specifically, there is a question as to whether Dr. Pratley was confused as to the
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`source of information he received from Registrant or whether Dr. Pratley’s reference to
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`“somebody” shows that he knew a party other that Petitioner was using a V-GO mark.
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`6.
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`Petitioner has failed to present evidence for other factors relevant to the lack of a
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`likelihood of confusion.
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`Petitioner has provided no evidence related to (i) the fame of the prior mark, (ii) the
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`number and nature of similar marks in use on similar goods, (iii) the variety of goods on which a
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`mark is or is not used, (iv) and the extent of potential confusion, i.e., whether de minimis or
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`substantial. Genuine issues of material facts relevant to these omitted factors exist which compel
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`denial of Petitioner’s Motion for Summary Judgment.
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`Upon an examination of the various factors which would establish a likelihood of
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`confusion, it is clear Petitioner has submitted no evidence to support his case for a majority of
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`the factors. For those few factors for which Petitioner has submitted evidence or argument,
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`genuine issues of material facts exist which compel denial of Petitioner’s Motion for Summary
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`Judgment. See Sports Authority, Inc. v. Prime Hospitality Corp., 89 F.3d 955, 39 U.S.P.Q.2d
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`1511 (2d Cir. 1996) (where five of the eight Polaroid factors weighed in favor of plaintiff and
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`three in favor of defendant, the court held that it was error for the district court to dismiss the
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`case on summary judgment.)
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`IV. CONCLUSION
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`VGo Communications, Inc.’s Opposition to Valeritas, Inc.’s Motion for Summary
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`Judgment has raised several contested issues of material fact. The unresolved facts relating to
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`likelihood of confusion confirms that Petitioner’s Motion for Summary Judgment should be
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`denied.
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`VGo Communications. Inc..
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`By its attorneys,
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` /John V. Hobgood/
`____________________________________
`Michael J. Bevilacqua
`Barbara A. Barakat
`John V. Hobgood
`Wilmer Cutler Pickering Hale and Dorr LLP
`60 State Street
`Boston, Massachusetts 02109
`(617) 526-6000
`
`December 15, 2010
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`Certificate Of Service
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`I certify that a true copy of the foregoing Registrant’s Opposition to Petitioner’s Motion
`for Summary Judgment and Memorandum in Support Thereof is being served by first-class mail,
`postage-prepaid, this 15th day of December, 2014,