Medical Device Manufacturer · US , North Attleboro , MA

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

4 submissions · 4 cleared · Since 1998

Total

Cleared

Denied

Neotonus, Inc. has 4 FDA 510(k) cleared medical devices. Based in North Attleboro, US.

Historical record: 4 cleared submissions from 1998 to 2001. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Neotonus, Inc.

4 devices

1-4 of 4