In Re PT MEDISAFE TECHNOLOGIES

U.S. Court of Appeals for the Federal Circuit

In Re PT MEDISAFE TECHNOLOGIES

Opinion

Case: 23-1573   Document: 48    Page: 1    Filed: 04/29/2025




   United States Court of Appeals
       for the Federal Circuit
                 ______________________

       IN RE: PT MEDISAFE TECHNOLOGIES,
                       Appellant
                ______________________

                       2023-1573
                 ______________________

     Appeal from the United States Patent and Trademark
 Office, Trademark Trial and Appeal Board in No.
 88083209.
                  ______________________

                 Decided: April 29, 2025
                 ______________________

     PERRY R. CLARK, Law Offices of Perry R. Clark, Palo
 Alto, CA, argued for appellant.

    CHRISTINA J. HIEBER, Office of the Solicitor, United
 States Patent and Trademark Office, Alexandria, VA, ar-
 gued for appellee Coke Morgan Stewart. Also represented
 by ERICA JEUNG DICKEY, ROBERT JAMES LAVACHE, AMY J.
 NELSON.
                  ______________________

   Before PROST, CLEVENGER, and STARK, Circuit Judges.
 STARK, Circuit Judge.
      PT Medisafe Technologies (“Medisafe”) appeals from a
 decision of the United States Patent and Trademark Of-
 fice’s (“PTO”) Trademark Trial and Appeal Board (“Board”)
 denying registration of its proposed mark. Because the
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 2                          IN RE: PT MEDISAFE TECHNOLOGIES




 Board applied the correct test for determining whether a
 color mark is generic, and substantial evidence supports
 the Board’s determination that Medisafe’s proposed mark
 is generic, we affirm.
                              I
      Medisafe, a medical glove manufacturer and distribu-
 tor, applied to the PTO for registration of a color mark for
 use on medical examination gloves.           The operative
 amended version of Medisafe’s application describes the
 proposed mark as “the color dark green (Pantone 3285 c) as
 applied to the entire surface of the goods which consist of
 chloroprene examination gloves.” J.A. 247. The applica-
 tion included a drawing of the mark, reproduced below (the
 broken line shows the positioning of the mark but is not
 part of it), and was accompanied by a specimen, also shown
 below:




 J.A. 252-53.
     Upon review of Medisafe’s initial application, the
 PTO’s examining attorney found that the dark green color
 was not inherently distinctive, so the proposed mark could
 not be placed on the principal or supplemental register
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 IN RE: PT MEDISAFE TECHNOLOGIES                           3



 without a showing that it had acquired distinctiveness. 1
 Medisafe attempted to make such a showing by providing
 the examiner with a declaration from Medisafe’s Executive
 Vice President and promotional literature. At the exam-
 iner’s request, Medisafe also submitted “[c]olor photo-
 graphs and color advertisements showing competitive
 goods in [its] industry.” J.A. 99. After reviewing these ma-
 terials, the examining attorney determined that Medisafe’s
 proposed color mark was generic and had not acquired dis-
 tinctiveness with respect to Medisafe’s goods. 2
     Medisafe responded to this rejection by trying again to
 prove that its mark had acquired distinctiveness, including
 by submitting additional declarations. The examining at-
 torney remained unpersuaded and issued a final decision,
 finding Medisafe’s proposed mark was generic, that Medis-
 afe had failed to prove acquired distinctiveness, and the
 mark could not be placed on the principal register. The ex-
 amining attorney further refused Medisafe’s alternative
 request to register its mark on the supplemental register.
 J.A. 498 (finding mark generic and “thus incapable of dis-
 tinguishing applicant’s goods”); see also J.A. 620.
     In determining that Medisafe’s color mark was generic,
 the examining attorney relied on the two-step test we orig-
 inally set forth in H. Marvin Ginn Corp. v. International


    1    Trademarks used in commerce may be placed on
 the principal register under 
15 U.S.C. § 1051
(a)(1). Marks
 “capable of distinguishing [the] applicant’s goods or ser-
 vices and not registrable on the principal register” may be
 placed on the supplemental register under 
15 U.S.C. § 1091
(a). See Matal v. Tam, 
582 U.S. 218, 224-25
 (2017).

    2     “[A] ‘generic’ term names a ‘class’ of good or ser-
 vices, rather than any particular feature or exemplification
 of the class.” United States PTO v. Booking.com B.V.,
 
591 U.S. 549, 556
 (2020).
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 4                           IN RE: PT MEDISAFE TECHNOLOGIES




 Ass’n of Fire Chiefs, Inc., 
782 F.2d 987, 990
 (Fed. Cir.
 1986): “First, what is the genus of goods or services at is-
 sue? Second, is the term sought to be registered or retained
 on the register understood by the relevant public primarily
 to refer to that genus of goods or services?” J.A. 274; see
 also J.A. 206.
     Medisafe appealed to the Board. In evaluating the ex-
 amining attorney’s genericness determination, the Board
 applied a “slight variation” of our Marvin Ginn test, tailor-
 ing the analysis to color marks. J.A. 4-5. This modified
 test had first been set out in the Board’s precedential deci-
 sion in Milwaukee Electric Tool Corp. v. Freud America,
 Inc., 
2019 WL 6522400
 (T.T.A.B. Dec. 2, 2019). Milwaukee
 states:
         We further believe it is appropriate to ap-
         ply a two-step inquiry to determine gener-
         icness of a single color similar to the
         inquiry we would apply to word marks and
         other kinds of trade dress, where we [(i)]
         first consider the genus of goods or services
         at issue, and [(ii)] second consider whether
         the color sought to be registered or retained
         on the register is understood by the rele-
         vant public primarily as a category or type
         of trade dress for that genus of goods or ser-
         vices. . . . Accordingly, we will identify the
         appropriate genus of goods and then deter-
         mine whether the color . . . is so common
         within the relevant genus that consumers
         would primarily associate it with the genus
         rather than as indicating a unique source
         of goods within the genus.
 
Id. at *9
.
     Applying the Milwaukee test, the Board rejected
 Medisafe’s proposed genus, which would have consisted of
 only gloves sold to authorized resellers, and instead defined
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 IN RE: PT MEDISAFE TECHNOLOGIES                             5



 the applicable genus as all “chloroprene medical examina-
 tion gloves.” J.A. 8. At the second step, the Board agreed
 with the examining attorney that the relevant public in-
 cludes “all such people or businesses who do or may pur-
 chase chloroprene medical examination gloves.” J.A. 12.
     Considering the entire record, the Board then agreed
 with the examining attorney that Medisafe’s color mark is
 generic because it “is so common in the chloroprene medical
 examination glove industry that it cannot identify a single
 source.” J.A. 45. The Board pointed to, for example,
 screenshots of websites selling, under third-party marks,
 “chloroprene/neoprene medical examination gloves in the
 same or nearly the same dark green color as in [the] pro-
 posed mark.” J.A. 13. While Medisafe claimed to be the
 manufacturer behind 15 of the screenshot examples,
 Medisafe made no such claim as to the other 10. The Board
 found all 25 screenshots to be probative of genericness be-
 cause “[t]he relevant consumer – even including unspeci-
 fied ‘authorized resellers’ – could be exposed to . . . gloves
 that appear under a large number of third-party marks
 without identifying [Medisafe] as the source or manufac-
 turer.” J.A. 14.
     The Board also evaluated Medisafe’s evidence that
 manufacturers make gloves in other colors besides the dark
 green of Medisafe’s proposed mark. It also considered cus-
 tomer declarations and a survey submitted by Medisafe.
 The Board placed little weight on this evidence because the
 other color gloves were not probative of whether the color
 Medisafe used is generic, the declarations were not “suffi-
 ciently representative or convincing of the relevant con-
 sumer perception of the proposed mark in general to carry
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 6                          IN RE: PT MEDISAFE TECHNOLOGIES




 much weight,” and the survey was “so flawed as to be enti-
 tled to no probative weight.” J.A. 40, 44. 3
      The Board’s genericness determination “serves as an
 absolute bar to registration.” J.A. 45. Nonetheless, like the
 examining attorney, the Board proceeded to consider ac-
 quired distinctiveness, agreeing that Medisafe had failed
 to meet its burden on this ground as well. Thus, the Board
 affirmed the examining attorney’s refusal to enter the pro-
 posed mark on either the principal or supplemental regis-
 ters.
     Medisafe timely appealed. We have jurisdiction pursu-
 ant to 
28 U.S.C. § 1295
(a)(4)(B).
                              II
     We review the Board’s legal conclusions de novo and its
 factual findings for substantial evidence. See In re Cordua
 Rests., Inc., 
823 F.3d 594, 599
 (Fed. Cir. 2016). Substantial
 evidence is “such relevant evidence as a reasonable mind
 might accept as adequate to support a conclusion.” Consol.
 Edison Co. v. NLRB, 
305 U.S. 197, 217
 (1938). Whether
 the Board applied the proper test in assessing whether a
 mark is generic is a question of law, but “whether a partic-
 ular mark is generic under the applicable standard is a
 question of fact, which we review for substantial evidence.”
 In re Cordua Rests., 
823 F.3d at 599
.



     3   The Board explained that the survey was adminis-
 tered by Medisafe’s counsel, not a survey expert; consisted
 of leading questions (e.g., “How long have you purchased
 the Medisafe dark green chloroprene glove, shown be-
 low?”); was sent to only six respondents, all of whom were
 part of Medisafe’s established customer base; and only
 three of those six respondents submitted responses – one
 of whom responded that she did not consider Medisafe’s
 color mark to be distinctive. J.A. 41; see also J.A. 42-44.
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 IN RE: PT MEDISAFE TECHNOLOGIES                            7



      To refuse registration based on a proposed mark being
 generic, the examining attorney must “establish a prima
 facie case that a term is generic.” Trademark Manual of
 Examining Procedure (“TMEP”) § 1209.01(c)(i) (2022).
 Thereafter, “the burden shifts to the applicant to come for-
 ward with evidence to rebut the prima facie case.” In re
 Pacer Tech., 
338 F.3d 1348, 1350
 (Fed. Cir. 2003). Then
 the Board, in reviewing an examining attorney’s refusal to
 register a mark, considers the full record and reaches its
 own conclusion as to whether the examiner made out a
 prima facie case and, if so, whether the applicant rebutted
 it, which may be accomplished by proving the mark had
 acquired distinctiveness. See In re Steelbuilding.com,
 
415 F.3d 1293, 1299
 (Fed. Cir. 2005); see also In re Oetiker,
 
977 F.2d 1443, 1445
 (Fed. Cir. 1992) (“In reviewing the ex-
 aminer’s decision on appeal, the Board [of Patent Appeals
 and Interferences] must necessarily weigh all of the evi-
 dence and argument.”). We review for substantial evidence
 the Board’s findings as to the prima facie case and whether
 it was rebutted by the applicant. See In re Hotels.com, L.P.,
 
573 F.3d 1300, 1301-02
 (Fed. Cir. 2009); see also In re Pacer
 Tech., 
338 F.3d at 1352
. 4



     4    Medisafe mistakenly suggests that on appeal the
 Board has a burden of proof and that this burden is to show
 by clear and convincing evidence that the proposed mark is
 generic. See Open. Br. at 10, 29. As the PTO correctly
 points out, the Board is a reviewing body, not a litigant,
 and has no burden of proof. See Resp. Br. at 18. Moreover,
 we have never held that the examining attorney must find
 genericness by clear and convincing evidence. A poten-
 tially confusing reference to “clear evidence” in the TMEP,
 which we referenced in In re Hotels.com, 
573 F.3d at 1302
,
 has recently been clarified and no longer suggests a clear
 and convincing evidence burden, compare TMEP
 § 1209.01(c)(i) (2021), with TMEP § 1209.01(c)(i) (2022).
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 8                          IN RE: PT MEDISAFE TECHNOLOGIES




                             III
     Medisafe argues that the Board applied the wrong le-
 gal standard for assessing whether a color mark is generic.
 Medisafe further contends that the Board’s finding that its
 proposed mark is generic is not supported by substantial
 evidence. We disagree on both points, as we explain below.
                              A
     In evaluating whether Medisafe’s proposed color mark
 is generic, the Board applied the two-part test it had set
 out in Milwaukee Electric Tool, 
2019 WL 6522400
, at *9.
 That test was itself a modification of our H. Marvin Ginn
 test, which had not expressly considered color marks. We
 agree with the Board that the Milwaukee test is appropri-
 ate and hereby adopt it.
     In H. Marvin Ginn, 
782 F.2d at 988
, we reviewed the
 Board’s cancellation of the mark FIRE CHIEF for a maga-
 zine directed to the field of firefighting. The Board had
 found the mark generic, but we reversed. See 
id. at 989, 991
. In doing so, we explained that the Board’s analysis,
 which was based primarily on cases relating to marks as-
 sociated with magazines, was too narrow. See 
id. at 991
.
 We set out the appropriate legal standard as follows:
     Determining whether a mark is generic therefore
     involves a two-step inquiry: First, what is the ge-
     nus of goods or services at issue? Second, is the
     term sought to be registered or retained on the reg-
     ister understood by the relevant public primarily to
     refer to that genus of goods or services?
 
Id. at 990
. While the facts of H. Marvin Ginn did not re-
 quire us to consider color marks, we articulated our test as
 applying to “mark[s],” without limitation as to their type.
     More than three decades later, in Milwaukee, the
 Board confronted the issue of whether a color mark was ge-
 neric. Expressly relying on H. Marvin Ginn, the Board
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 IN RE: PT MEDISAFE TECHNOLOGIES                               9



 found it “appropriate to apply a two-step inquiry to deter-
 mine genericness of a single color similar to the inquiry we
 apply to word marks and other kinds of trade dress.”
 
2019 WL 6522400
, at *9. The Milwaukee test begins with
 the same inquiry as H. Marvin Ginn, requiring identifica-
 tion of the genus of goods or services at issue. Compare
 
2019 WL 6522400
, at *9, with 
782 F.2d at 990
. The Mil-
 waukee test then slightly modifies the second-step inquiry
 to tailor it to color marks. Whereas H. Marvin Ginn asks
 whether “the term sought to be registered or retained on
 the register [is] understood by the relevant public primar-
 ily to refer to [a] genus of goods or services,” 
782 F.2d at 990
 (emphasis added), Milwaukee asks “whether the color
 sought to be registered . . . is understood by the relevant
 public primarily as a category or type of trade dress for [a]
 genus of goods or services,” 
2019 WL 6522400
, at *9 (em-
 phasis added).
     Here, the Board applied the Milwaukee test to Medis-
 afe’s proposed color mark. See J.A. 6-13. Medisafe asserts
 this was legal error. We disagree.
      The Milwaukee test is entirely consistent with H.
 Marvin Ginn. Milwaukee minimally, but appropriately,
 modifies H. Marvin Ginn to address the specific circum-
 stances of a color mark being assessed for genericness. See
 generally Qualitex Co. v. Jacobson Prods. Co., 
514 U.S. 159, 164
 (1995) (“It is the source-distinguishing ability of a
 mark – not its ontological status as color, shape, fragrance,
 word, or sign – that permits it to serve [the] basic purposes
 [of trademark law].”).
     Medisafe’s principal attack on the Milwaukee test is
 that it purportedly ignores statutory language, which al-
 lows for cancellation of a mark for genericness only where
 that mark is a “generic name.” See, e.g., Open. Br. at 17
 (“There are many problems with the [Board’s] Milwaukee
 test but the most obvious is that ‘trade dress’ is not the
 name of a genus of goods or services . . . .”). Medisafe
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 10                           IN RE: PT MEDISAFE TECHNOLOGIES




 predicates this contention on 
15 U.S.C. § 1064
(3), which
 provides that a registered mark may be cancelled “[a]t any
 time if the registered mark becomes the generic name for
 the goods or services, or a portion thereof, for which it is
 registered” (emphasis added). According to Medisafe, this
 “generic name” requirement applies equally to all types of
 marks, meaning that trade dress – including a color mark
 – may, like a word mark, be found generic only if it is a
 “generic name” for the goods with which it is used.
      We considered, and rejected, essentially this same con-
 tention in Sunrise Jewelry Manufacturing Corp. v. Fred
 S.A., 
175 F.3d 1322
 (Fed. Cir. 1999). In Sunrise Jewelry,
 the Board had concluded that a registered mark of a “me-
 tallic nautical rope design” for clocks, watches, and jewelry
 could not be cancelled as generic because, as trade dress,
 the design could not be a “generic name.” 
Id. at 1323, 1325
.
 We disagreed with the contention that “the plain meaning
 of ‘generic name’ in § 1064(3) excludes trade dress” and
 held, instead, that the statutory language “must be read
 expansively to encompass anything that has the potential
 but fails to serve as an indicator of source, such as . . . trade
 dress.” Id. at 1325-26. “Any narrower interpretation of ‘ge-
 neric name’ would,” we explained, accord trade dress “more
 protection than a word mark under the Lanham Act,” and
 thereby “directly contravene the purpose of the Lanham
 Act.” Id. We reiterate, as we held in Sunrise Jewelry, id.
 at 1326, “trade dress,” including a color mark, “that cannot
 serve as an indicator of source is generic and unprotecta-
 ble.” 5




      5  At oral argument, counsel for Medisafe conceded
 that a color mark can be generic. See Oral Argument at
 2:32-2:44,   available    at   https://oralarguments.cafc.
 uscourts.gov/default.aspx?fl=23-1573_08082024.mp3.
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 IN RE: PT MEDISAFE TECHNOLOGIES                             11



                               B
     Applying the Milwaukee test, we conclude that sub-
 stantial evidence supports the Board’s determination that
 Medisafe’s proposed color mark is generic.
      At the first step of the inquiry, the Board identified the
 genus of goods at issue as “chloroprene medical examina-
 tion gloves.” J.A. 8. Substantial evidence supports this
 finding, including the fact that Medisafe’s initial applica-
 tion identified the goods for which it sought to register its
 marks as “[m]edical examination gloves.” J.A. 53. The
 Board did not err in rejecting Medisafe’s amended applica-
 tion’s narrowing of the goods at issue to “chloroprene med-
 ical gloves sold only to authorized resellers.” J.A. 10-11
 (emphasis added). 6 The Board is not compelled to accept
 an applicant’s proposed definition of the applicable genus,
 and was right not to “limit the universe of chloroprene med-
 ical examination gloves under evidentiary consideration to
 [Medisafe’s] own products.” J.A. 10-11 (citing In re
 i.am.symbolic, LLC, 
866 F.3d 1315, 1324
 (Fed. Cir. 2017)
 (finding no error where Board refused to limit identifica-
 tion of goods to products “associated with” singer
 will.i.am)).
     Turning to the second step, substantial evidence sup-
 ports the Board’s finding, which it reached after reviewing
 the entire record, that Medisafe’s color mark “is so common
 in the chloroprene medical examination glove industry that



     6    Although Medisafe frames its “authorized re-
 sellers” argument as directed to the definition of the rele-
 vant public, part of the second step of the genericness
 inquiry, we view Medisafe’s argument as challenging the
 Board’s exclusion of the authorized retailer limitation from
 the genus of goods at issue. At either the first or second
 step of the Milwaukee test, Medisafe points to no meritori-
 ous reason to include its “authorized resellers” limitation.
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 12                          IN RE: PT MEDISAFE TECHNOLOGIES




 it cannot identify a single source” and is, therefore, generic.
 J.A. 45. This evidence includes screenshots of third-party
 websites showing unaffiliated sellers of “chloroprene/neo-
 prene medical examination gloves in the same or nearly the
 same dark green color as in [the] proposed mark,” J.A. 13;
 customer declarations, which the Board reasonably found
 are not “sufficiently representative or convincing of the rel-
 evant consumer perception of the proposed mark in general
 to carry much weight,” especially because the “declarations
 are few in number, identical in form (which, while not fatal,
 makes them less persuasive), and relatively conclusory,”
 J.A. 40; and the survey, whose “flaws” the Board reasona-
 bly found “too numerous to detail” and include that they
 were “conducted by Applicant’s counsel,” who was not qual-
 ified as a survey expert, was given “to a small subset of Ap-
 plicant’s established customer base,” and relied on
 “leading” questions (nevertheless resulting in one of three
 respondents “indicat[ing] that Applicant’s proposed color
 mark was not distinctive in the industry”), J.A. 41-44. 7
      In sum, as the Board recognized, while a color mark
 may serve as a source indicator, substantial evidence sup-
 ports the Board’s finding that Medisafe’s proposed mark
 failed to do so. J.A. 39 (“There is no question that color
 marks generally are capable of serving as source-indicators
 – that is not the ground for refusal here. Rather, the rele-
 vant inquiry focuses on the consumer perception of the



      7  Medisafe points out that the Board reproduced in
 its opinion a different specimen of its mark than what
 Medisafe’s survey used. Open. Br. at 34-35 (comparing J.A.
 252 with J.A. 43); Reply Br. at 17-18. This error cannot
 have had any impact on the Board’s analysis and, hence, is
 harmless. See generally Swagway, LLC v. Int’l Trade
 Comm’n, 
934 F.3d 1332, 1343
 (Fed. Cir. 2019) (finding that
 error was harmless in absence of showing of any prejudice).
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 IN RE: PT MEDISAFE TECHNOLOGIES                            13



 particular color at issue as to the genus set by Applicant’s
 identified goods.”). Therefore, we affirm the Board’s deter-
 mination that Medisafe’s proposed mark is generic and,
 hence, ineligible for registry on either the principal or sup-
 plemental registers.
                              IV
     We have considered Medisafe’s remaining arguments
 and find them either unnecessary to address or unpersua-
 sive. 8 For the reasons stated above, we affirm the Board’s
 decision.
                         AFFIRMED




       8      We do not reach Medisafe’s challenges to the
 Board’s finding that it failed to prove acquired distinctive-
 ness. Because a generic mark is “the ultimate in descrip-
 tiveness,” it “cannot acquire distinctiveness.” Real Foods
 Pty Ltd. v. Frito-Lay N. Am., Inc., 
906 F.3d 965
, 972 n.3
 (Fed. Cir. 2018).


Reference

Status
Published