Medical Device Manufacturer · US , Anaheim , CA

Kmi Kolster Methods, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1999

Total

Cleared

Denied

Kmi Kolster Methods, Inc. has 6 FDA 510(k) cleared medical devices. Based in Anaheim, US.

Historical record: 6 cleared submissions from 1999 to 2006. Primary specialty: General & Plastic Surgery.

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

Kmi Kolster Methods, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kmi Kolster Methods, Inc.

6 devices

1-6 of 6