ANTARMA LLC

FDA Device Registration & Listing · New York, NY, US · Registration 3014117096

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014117096
FEI Number
3014117096
Entity Name
ANTARMA LLC
City/State/Country
New York, NY, US
Establishment Address
276 5th Ave Rm 704, New York, NY 10001, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Antarma LLC dba Golnit Sutures (Owner Number: 10056317)
Owner / Operator Contact Address
276 5th Ave Rm 704, New York, NY 10001, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K163049
PMA Number
N/A

All Registered Proprietary Names

Golnit Nylon Monofilament Suture Golnit PTFE Suture Golnit PTFE Sutures

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAR Suture, Nonabsorbable, Synthetic, Polyamide General, Plastic Surgery Class 2 878.5020 2022-05-28
NBY Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene General, Plastic Surgery Class 2 878.5035 2022-09-22
NBY Suture, Surgical, Nonabsorbable, Expanded, Polytetraflouroethylene General, Plastic Surgery Class 2 878.5035 2017-11-28

Official Correspondent

Armine Badalyan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Antarma LLC dba Golnit Sutures
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2009 Surgical Specialties Corp 2
3-0 Black Mono Nylon Suture, 12 units per box. product number 925B. The product intended for use in general soft tissue approximation and/or ligation including use in ophthalmic procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014117096. Last updated year: 2026. Please use registration number 3014117096 when referencing this establishment in official correspondence.
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