Medical Device Manufacturer · US , Walker , MI

Minnetonka, Inc. - FDA 510(k) Cleared Devices

4 submissions · 2 cleared · Since 1983

Total

Cleared

Denied

Minnetonka, Inc. has 2 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 2 cleared submissions from 1983 to 1989. Primary specialty: General & Plastic Surgery.

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

Minnetonka, 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 - Minnetonka, Inc.

4 devices

1-4 of 4