Cro, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cro, LLC - FDA 510(k) Cleared Devices
Recent clearances: AIRO Suction Unit (AIRO-01)
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