Certain Nasal Devices and Components Thereof; Notice of Institution of Investigation, 13781-13782 [2025-05116]

Download as PDF Federal Register / Vol. 90, No. 57 / Wednesday, March 26, 2025 / Notices Issued: March 21, 2025. Sharon Bellamy, Supervisory Hearings and Information Officer. by accessing its internet server at https://www.usitc.gov. FOR FURTHER INFORMATION CONTACT: [FR Doc. 2025–05114 Filed 3–25–25; 8:45 am] BILLING CODE 7020–02–P INTERNATIONAL TRADE COMMISSION [Investigation No. 337–TA–1444] Certain Nasal Devices and Components Thereof; Notice of Institution of Investigation U.S. International Trade Commission. ACTION: Notice. AGENCY: Notice is hereby given that a complaint was filed with the U.S. International Trade Commission on February 18, 2025, under section 337 of the Tariff Act of 1930, as amended, on behalf of Aardvark Medical Inc. of Denton, Texas. A supplement was filed on February 25, 2025. The complaint, as supplemented, alleges violations of section 337 based upon the importation into the United States, the sale for importation, and the sale within the United States after importation of certain nasal devices and components thereof by reason of the infringement of certain claims of U.S. Patent No. 9,750,856 (‘‘the ’856 patent’’); U.S. Patent No. 11,318,234 (‘‘the ’234 patent’’); U.S. Patent No. 11,883,009 (‘‘the ’009 patent’’); U.S. Patent No. 11,883,010 (‘‘the ’010 patent’’); and U.S. Patent No. 11,889,995 (‘‘the ’995 patent’’). The complaint, as supplemented, further alleges that an industry in the United States exists as required by the applicable Federal Statute. The complainant requests that the Commission institute an investigation and, after the investigation, issue a limited exclusion order and cease and desist orders. ADDRESSES: The complaint, except for any confidential information contained therein, may be viewed on the Commission’s electronic docket (EDIS) at https://edis.usitc.gov. For help accessing EDIS, please email EDIS3Help@usitc.gov. Hearing impaired individuals are advised that information on this matter can be obtained by contacting the Commission’s TDD terminal on (202) 205–1810. Persons with mobility impairments who will need special assistance in gaining access to the Commission should contact the Office of the Secretary at (202) 205– 2000. General information concerning the Commission may also be obtained khammond on DSK9W7S144PROD with NOTICES SUMMARY: VerDate Sep<11>2014 16:57 Mar 25, 2025 Jkt 265001 Susan Orndoff, The Office of Docket Services, U.S. International Trade Commission, telephone (202) 205–1802. SUPPLEMENTARY INFORMATION: Authority: The authority for institution of this investigation is contained in section 337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337, and in section 210.10 of the Commission’s Rules of Practice and Procedure, 19 CFR 210.10 (2024). Scope of Investigation: Having considered the complaint, the U.S. International Trade Commission, on March 20, 2025, ordered that— (1) Pursuant to subsection (b) of section 337 of the Tariff Act of 1930, as amended, an investigation be instituted to determine whether there is a violation of subsection (a)(1)(B) of section 337 in the importation into the United States, the sale for importation, or the sale within the United States after importation of certain products identified in paragraph (2) by reason of infringement of one or more of claims 1–5, 7–14, and 16–19 of the ’856 patent; claims 1–4, 6, 8–12, 14–17, 21–24, 27, and 28 of the ’234 patent; 1–3, 6–8, 10– 12, 16–18, 21, 22, and 28 of the ’009 patent; claims 1–8, 10–15, and 17–22 of the ’010 patent; and claims 1–9, 12–21, 23, 24, and 26 of the ’995 patent, and whether an industry in the United States exists as required by subsection (a)(2) of section 337; (2) Pursuant to section 210.10(b)(1) of the Commission’s Rules of Practice and Procedure, 19 CFR 210.10(b)(1), the plain language description of the accused products or category of accused products, which defines the scope of the investigation, is ‘‘nasal irrigation and aspiration devices and components thereof’’; 1 (3) For the purpose of the investigation so instituted, the following are hereby named as parties upon which this notice of investigation shall be served: The complainant is: Aardvark Medical Inc., 204 Cardinal Drive, Denton, Texas 76209 1 In this plain English statement of the scope of investigation, ‘‘components thereof’’ is included pursuant to the allegations in the complaint. To the extent that the Complainant has included such an allegation based upon a concern regarding specific components, the Complainant should, during the course of this investigation, seek adjudication and specifically identify the components of the claimed invention sought for exclusion. The lack of adjudication of specific components, however, would not affect any later ability to adjudicate and remedy circumvention through the importation of components with additional enforcement actions. PO 00000 Frm 00055 Fmt 4703 Sfmt 4703 13781 (b) The respondents are the following entities alleged to be in violation of section 337, and are the parties upon which the complaint is to be served: Xiamenximier Electronic Commerce Co., Ltd (d/b/a Cenny), Room 203, Building 1070–2, Caitangshe, Huli District, Xiamen City, Fujian China 361000 Xia Men Deng Jia E-Commerce Co., Ltd., (d/b/a Ronfnea), Room 101, No. 1070– 1, Caitangshe, Xiamen, Huli District, Fujian, China 361006, Chongqing Moffy Innovation Technology, Co., Ltd., No. 292, Jingdongfang Rd., Beibei Dist., Chongqing City, 400714 China Guangdong XINRUNTAO Technology, Co., Ltd., Room 1101–1102, Xingji Tower, Xinqiao, Bao’an Shenzhen, Guangdong, China Shenzhen Jun&Liang Media Tech Limited, Building 16, Dongcai Industrial Park, Gushu Village, Xixiang Town, Bao’an District, Shenzhen, China 518102 RhinoSystems, Inc., 1 American Road, Suite 1100, Brooklyn, Ohio 44144 Spa Sciences LP, 584 NW University Blvd., Suite 600, Port St. Lucie, Florida 34986 (4) For the investigation so instituted, the Chief Administrative Law Judge, U.S. International Trade Commission, shall designate the presiding Administrative Law Judge. The Office of Unfair Import Investigations will not participate as a party in this investigation. Responses to the complaint and the notice of investigation must be submitted by the named respondents in accordance with section 210.13 of the Commission’s Rules of Practice and Procedure, 19 CFR 210.13. Pursuant to 19 CFR 201.16(e) and 210.13(a), such responses will be considered by the Commission if received not later than 20 days after the date of service by the Commission of the complaint and the notice of investigation. Extensions of time for submitting responses to the complaint and the notice of investigation will not be granted unless good cause therefor is shown. Failure of a respondent to file a timely response to each allegation in the complaint and in this notice may be deemed to constitute a waiver of the right to appear and contest the allegations of the complaint and this notice, and to authorize the administrative law judge and the Commission, without further notice to the respondent, to find the facts to be as alleged in the complaint and this notice and to enter an initial determination and a final determination containing E:\FR\FM\26MRN1.SGM 26MRN1 13782 Federal Register / Vol. 90, No. 57 / Wednesday, March 26, 2025 / Notices such findings, and may result in the issuance of an exclusion order or a cease and desist order or both directed against the respondent. By order of the Commission. Issued: March 21, 2025. Sharon Bellamy, Supervisory Hearings and Information Officer. [FR Doc. 2025–05116 Filed 3–25–25; 8:45 am] BILLING CODE 7020–02–P DEPARTMENT OF JUSTICE Drug Enforcement Administration Administration, Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing should also be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this is notice that on February 11, 2025, Pharmaron Manufacturing Services (US) LLC, 498 Washington Street, Coventry, Rhode Island 02816, applied to be registered as an importer of the following basic class(es) of controlled substance(s): [Docket No. DEA–1514] Importer of Controlled Substances Application: Pharmaron Manufacturing Services (US) LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Pharmaron Manufacturing Services (US) LLC has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information. SUMMARY: Registered bulk manufacturers of the affected basic class(es), and applicants, therefore, may submit electronic comments on or objections to the issuance of the proposed registration on or before April 25, 2025. Such persons may also file a written request for a hearing on the application on or before April 25, 2025. ADDRESSES: The Drug Enforcement Administration requires that all comments be submitted electronically through the Federal eRulemaking Portal, which provides the ability to type short comments directly into the comment field on the web page or attach a file for lengthier comments. Please go to https://www.regulations.gov and follow the online instructions at that site for submitting comments. Upon submission of your comment, you will receive a Comment Tracking Number. Please be aware that submitted comments are not instantaneously available for public view on https://www.regulations.gov. If you have received a Comment Tracking Number, your comment has been successfully submitted and there is no need to resubmit the same comment. All requests for a hearing must be sent to: (1) Drug Enforcement Administration, Attn: Hearing Clerk/OALJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and (2) Drug Enforcement khammond on DSK9W7S144PROD with NOTICES DATES: VerDate Sep<11>2014 16:57 Mar 25, 2025 Jkt 265001 Controlled substance Dimethyltryptamine .......... Drug code Schedule 7435 I The company plans to import the above controlled substance for internal analytical use and to support technology transfer, further process, and subsequent production of Active Pharmaceutical Ingredient for sale to its customers. No other activity for this drug code is authorized for this registration. Approval of permit applications will occur only when the registrant’s business activity is consistent with what is authorized under 21 U.S.C. 952(a)(2). Authorization will not extend to the import of Food and Drug Administration-approved or nonapproved finished dosage forms for commercial sale. Matthew Strait, Deputy Assistant Administrator. [FR Doc. 2025–05056 Filed 3–25–25; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–1512] Bulk Manufacturer of Controlled Substances Application: Pharmaron Manufacturing Services (US), LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. electronic comments on or objections to the issuance of the proposed registration on or before May 27, 2025. Such persons may also file a written request for a hearing on the application on or before May 27, 2025. ADDRESSES: The Drug Enforcement Administration requires that all comments be submitted electronically through the Federal eRulemaking Portal, which provides the ability to type short comments directly into the comment field on the web page or attach a file for lengthier comments. Please go to https://www.regulations.gov and follow the online instructions at that site for submitting comments. Upon submission of your comment, you will receive a Comment Tracking Number. Please be aware that submitted comments are not instantaneously available for public view on https://www.regulations.gov. If you have received a Comment Tracking Number, your comment has been successfully submitted and there is no need to resubmit the same comment. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this is notice that on February 11, 2025, Pharmaron Manufacturing Services (US), LLC, 498 Washington Street, Coventry, Rhode Island 02816 applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): Controlled substance Dimethyltryptamine .... Oxymorphone ............ Noroxymorphone ....... Drug code 7435 9652 9668 Schedule I II II The company plans to bulk manufacture the listed controlled substances to produce material for clinical trials. No other activities for these drug codes are authorized for this registration. Matthew Strait, Deputy Assistant Administrator. [FR Doc. 2025–05055 Filed 3–25–25; 8:45 am] BILLING CODE P AGENCY: DEPARTMENT OF JUSTICE Drug Enforcement Administration Pharmaron Manufacturing Services (US), LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information. DATES: Registered bulk manufacturers of the affected basic class(es), and applicants, therefore, may submit SUMMARY: PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 [Docket No. DEA–1515] Bulk Manufacturer of Controlled Substances Application: Sterling Wisconsin, LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: E:\FR\FM\26MRN1.SGM 26MRN1

Agencies

[Federal Register Volume 90, Number 57 (Wednesday, March 26, 2025)]
[Notices]
[Pages 13781-13782]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-05116]


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INTERNATIONAL TRADE COMMISSION

[Investigation No. 337-TA-1444]


Certain Nasal Devices and Components Thereof; Notice of 
Institution of Investigation

AGENCY: U.S. International Trade Commission.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: Notice is hereby given that a complaint was filed with the 
U.S. International Trade Commission on February 18, 2025, under section 
337 of the Tariff Act of 1930, as amended, on behalf of Aardvark 
Medical Inc. of Denton, Texas. A supplement was filed on February 25, 
2025. The complaint, as supplemented, alleges violations of section 337 
based upon the importation into the United States, the sale for 
importation, and the sale within the United States after importation of 
certain nasal devices and components thereof by reason of the 
infringement of certain claims of U.S. Patent No. 9,750,856 (``the '856 
patent''); U.S. Patent No. 11,318,234 (``the '234 patent''); U.S. 
Patent No. 11,883,009 (``the '009 patent''); U.S. Patent No. 11,883,010 
(``the '010 patent''); and U.S. Patent No. 11,889,995 (``the '995 
patent''). The complaint, as supplemented, further alleges that an 
industry in the United States exists as required by the applicable 
Federal Statute. The complainant requests that the Commission institute 
an investigation and, after the investigation, issue a limited 
exclusion order and cease and desist orders.

ADDRESSES: The complaint, except for any confidential information 
contained therein, may be viewed on the Commission's electronic docket 
(EDIS) at https://edis.usitc.gov. For help accessing EDIS, please email 
[email protected]. Hearing impaired individuals are advised that 
information on this matter can be obtained by contacting the 
Commission's TDD terminal on (202) 205-1810. Persons with mobility 
impairments who will need special assistance in gaining access to the 
Commission should contact the Office of the Secretary at (202) 205-
2000. General information concerning the Commission may also be 
obtained by accessing its internet server at https://www.usitc.gov.

FOR FURTHER INFORMATION CONTACT: Susan Orndoff, The Office of Docket 
Services, U.S. International Trade Commission, telephone (202) 205-
1802.

SUPPLEMENTARY INFORMATION: 
    Authority: The authority for institution of this investigation is 
contained in section 337 of the Tariff Act of 1930, as amended, 19 
U.S.C. 1337, and in section 210.10 of the Commission's Rules of 
Practice and Procedure, 19 CFR 210.10 (2024).
    Scope of Investigation: Having considered the complaint, the U.S. 
International Trade Commission, on March 20, 2025, ordered that--
    (1) Pursuant to subsection (b) of section 337 of the Tariff Act of 
1930, as amended, an investigation be instituted to determine whether 
there is a violation of subsection (a)(1)(B) of section 337 in the 
importation into the United States, the sale for importation, or the 
sale within the United States after importation of certain products 
identified in paragraph (2) by reason of infringement of one or more of 
claims 1-5, 7-14, and 16-19 of the '856 patent; claims 1-4, 6, 8-12, 
14-17, 21-24, 27, and 28 of the '234 patent; 1-3, 6-8, 10-12, 16-18, 
21, 22, and 28 of the '009 patent; claims 1-8, 10-15, and 17-22 of the 
'010 patent; and claims 1-9, 12-21, 23, 24, and 26 of the '995 patent, 
and whether an industry in the United States exists as required by 
subsection (a)(2) of section 337;
    (2) Pursuant to section 210.10(b)(1) of the Commission's Rules of 
Practice and Procedure, 19 CFR 210.10(b)(1), the plain language 
description of the accused products or category of accused products, 
which defines the scope of the investigation, is ``nasal irrigation and 
aspiration devices and components thereof''; \1\
---------------------------------------------------------------------------

    \1\ In this plain English statement of the scope of 
investigation, ``components thereof'' is included pursuant to the 
allegations in the complaint. To the extent that the Complainant has 
included such an allegation based upon a concern regarding specific 
components, the Complainant should, during the course of this 
investigation, seek adjudication and specifically identify the 
components of the claimed invention sought for exclusion. The lack 
of adjudication of specific components, however, would not affect 
any later ability to adjudicate and remedy circumvention through the 
importation of components with additional enforcement actions.
---------------------------------------------------------------------------

    (3) For the purpose of the investigation so instituted, the 
following are hereby named as parties upon which this notice of 
investigation shall be served:
    The complainant is:
Aardvark Medical Inc., 204 Cardinal Drive, Denton, Texas 76209

    (b) The respondents are the following entities alleged to be in 
violation of section 337, and are the parties upon which the complaint 
is to be served:

Xiamenximier Electronic Commerce Co., Ltd (d/b/a Cenny), Room 203, 
Building 1070-2, Caitangshe, Huli District, Xiamen City, Fujian China 
361000
Xia Men Deng Jia E-Commerce Co., Ltd., (d/b/a Ronfnea), Room 101, No. 
1070-1, Caitangshe, Xiamen, Huli District, Fujian, China 361006, 
Chongqing Moffy Innovation Technology, Co., Ltd., No. 292, Jingdongfang 
Rd., Beibei Dist., Chongqing City, 400714 China
Guangdong XINRUNTAO Technology, Co., Ltd., Room 1101-1102, Xingji 
Tower, Xinqiao, Bao'an Shenzhen, Guangdong, China
Shenzhen Jun&Liang Media Tech Limited, Building 16, Dongcai Industrial 
Park, Gushu Village, Xixiang Town, Bao'an District, Shenzhen, China 
518102
RhinoSystems, Inc., 1 American Road, Suite 1100, Brooklyn, Ohio 44144
Spa Sciences LP, 584 NW University Blvd., Suite 600, Port St. Lucie, 
Florida 34986

    (4) For the investigation so instituted, the Chief Administrative 
Law Judge, U.S. International Trade Commission, shall designate the 
presiding Administrative Law Judge.
    The Office of Unfair Import Investigations will not participate as 
a party in this investigation.
    Responses to the complaint and the notice of investigation must be 
submitted by the named respondents in accordance with section 210.13 of 
the Commission's Rules of Practice and Procedure, 19 CFR 210.13. 
Pursuant to 19 CFR 201.16(e) and 210.13(a), such responses will be 
considered by the Commission if received not later than 20 days after 
the date of service by the Commission of the complaint and the notice 
of investigation. Extensions of time for submitting responses to the 
complaint and the notice of investigation will not be granted unless 
good cause therefor is shown.
    Failure of a respondent to file a timely response to each 
allegation in the complaint and in this notice may be deemed to 
constitute a waiver of the right to appear and contest the allegations 
of the complaint and this notice, and to authorize the administrative 
law judge and the Commission, without further notice to the respondent, 
to find the facts to be as alleged in the complaint and this notice and 
to enter an initial determination and a final determination containing

[[Page 13782]]

such findings, and may result in the issuance of an exclusion order or 
a cease and desist order or both directed against the respondent.

    By order of the Commission.

    Issued: March 21, 2025.
Sharon Bellamy,
Supervisory Hearings and Information Officer.
[FR Doc. 2025-05116 Filed 3-25-25; 8:45 am]
BILLING CODE 7020-02-P


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