Medical Device Manufacturer · CA , Laval Quebec

Tanses Technologies, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2016

Total

Cleared

Denied

Tanses Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Laval Quebec, CA.

Historical record: 3 cleared submissions from 2016 to 2018. Primary specialty: Physical Medicine.

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

FDA 510(k) Regulatory Record - Tanses Technologies, Inc.

3 devices

1-3 of 3