Peregrine Surgical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Peregrine Surgical, LLC - FDA 510(k) Cleared Devices
Recent clearances: Midfield Light Pipe, 23ga (3269.M06-00)
1
Total
1
Cleared
0
Denied
Peregrine Surgical, LLC has 1 FDA 510(k) cleared medical devices. Based in New Britain, US.
Latest FDA clearance: Aug 2024. Active since 2024. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Peregrine Surgical, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Peregrine Surgical, LLC
1 devices