Medical Device Manufacturer · US , Missoula , MT

Cro, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

Cro, LLC has 1 FDA 510(k) cleared medical devices. Based in Missoula, US.

Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Cro, LLC
1 devices
1-1 of 1
Filters