Medical Device Manufacturer · US , Pittsburgh , PA

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

22 submissions · 22 cleared · Since 2012
22
Total
22
Cleared
0
Denied

Blue Belt Technologies, Inc. has 22 FDA 510(k) cleared orthopedic devices. Based in Pittsburgh, US.

Latest FDA clearance: Mar 2026. Active since 2012.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Blue Belt Technologies, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Blue Belt Technologies, Inc.
22 devices
1-12 of 22
Filters