Peleton Surgical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Peleton Surgical - FDA 510(k) Cleared Devices
Recent clearances: Peleton Universal Single Use Power System and Attachments
1
Total
1
Cleared
0
Denied
Peleton Surgical has 1 FDA 510(k) cleared medical devices. Based in Scottsdale, US.
Latest FDA clearance: Apr 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Peleton Surgical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Peleton Surgical
1 devices