Medical Device Manufacturer · US , Washington , DC

Artimplant AB - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2003

Total

Cleared

Denied

Artimplant AB has 7 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 7 cleared submissions from 2003 to 2007. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Artimplant AB Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Artimplant AB

7 devices

1-7 of 7