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) cleared devices by Antarma, LLC Dba Golnit Sutures

2 devices

1-2 of 2