Medical Device Manufacturer · US , Ann Arbor , MI

Top Spins, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1997

Total

Cleared

Denied

Top Spins, Inc. has 3 FDA 510(k) cleared medical devices. Based in Ann Arbor, US.

Historical record: 3 cleared submissions from 1997 to 2016. Primary specialty: General Hospital.

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

FDA 510(k) Regulatory Record - Top Spins, Inc.

3 devices

1-3 of 3