Medical Device Manufacturer · US , Laguna Hills , CA

Vesitec Medical, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1993

Total

Cleared

Denied

Vesitec Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Laguna Hills, US.

Historical record: 3 cleared submissions from 1993 to 1994. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Vesitec Medical, Inc.

3 devices

1-3 of 3