Program Insite, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Program Insite, LLC - FDA 510(k) Cleared Devices
Recent clearances: Program insite® Powder-Free, Disposable Nitrile Exam Gloves
1
Total
1
Cleared
0
Denied
Program Insite, LLC has 1 FDA 510(k) cleared medical devices. Based in Olney, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Program Insite, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Program Insite, LLC
1 devices