Medical Device Manufacturer · US , Fullerton , CA

Kolster Methods - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1989

Total

Cleared

Denied

Kolster Methods has 3 FDA 510(k) cleared medical devices. Based in Fullerton, US.

Historical record: 3 cleared submissions from 1989 to 1994. Primary specialty: General & Plastic Surgery.

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

3 devices

1–3 of 3