Medical Device Manufacturer · US , New York , NY

Antarma, LLC Dba Golnit Sutures - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019

Total

Cleared

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

1-2 of 2