Medical Device Manufacturer · US , Mchenry , IL

Prothia USA, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1982

Total

Cleared

Denied

Prothia USA, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 5 cleared submissions from 1982 to 1983. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Prothia USA, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Prothia USA, Inc.

5 devices

1-5 of 5