Cork Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cork Medical - FDA 510(k) Cleared Devices
Recent clearances: Nisus NPWT Canister 500-mL (CPC-500), Nisus ONE Negative Pressure Wound Therapy System (OCMPP-100), VERSA Negative Pressure Wound Therapy System (VCMPP-100)
4
Total
4
Cleared
0
Denied
Cork Medical has 4 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Latest FDA clearance: May 2026. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Cork Medical Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cork Medical
4 devices
Cleared
May 21, 2026
Nisus NPWT Canister 500-mL (CPC-500)
General & Plastic Surgery
31d
Cleared
Jun 27, 2025
Nisus ONE Negative Pressure Wound Therapy System (OCMPP-100)
General & Plastic Surgery
270d
Cleared
Aug 21, 2024
VERSA Negative Pressure Wound Therapy System (VCMPP-100)
General & Plastic Surgery
125d
Cleared
Dec 06, 2023
Cork Medical VERSA Negative Pressure Wound System (VCMPP-100)
General & Plastic Surgery
271d