Antarma, LLC Dba Golnit Sutures is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Antarma, LLC Dba Golnit Sutures - FDA 510(k) Cleared Devices
Recent clearances: Golnit Nylon Monofilament Suture, GOLNIT Non-aborbable PTFE Surgical Suture
2
Total
2
Cleared
0
Denied
Antarma, LLC Dba Golnit Sutures has 2 FDA 510(k) cleared medical devices. Based in New York, US.
Last cleared in 2022. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Antarma, LLC Dba Golnit Sutures Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Antarma, LLC Dba Golnit Sutures
2 devices