FDA applicant
Antarma, LLC Dba Golnit Sutures
FDA records 3 decisions for Antarma, LLC Dba Golnit Sutures (New York, NY) from 2017 to 2022: 3 510(k) clearances. Most are in product codes NBY (Suture, Surgical, Nonabsorbable, Expanded…) and GAR (Suture, Nonabsorbable, Synthetic, Polyamide). Its devices cite 6 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Antarma Dba Golnit Sutures”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Antarma, LLC Dba Golnit Sutures’s devices, and how often a recall has named them.
FDA decisions per year
1in 2022
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Antarma, LLC Dba Golnit Sutures’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report