Unipack Medical Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unipack Medical Corporation - FDA 510(k) Cleared Devices
Recent clearances: UNiPACK Barrier Sleeve and Barrier Film and UNiGLIDE Barrier Envelope
1
Total
1
Cleared
0
Denied
Unipack Medical Corporation has 1 FDA 510(k) cleared medical devices. Based in Santa Fe Springs, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Unipack Medical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Unipack Medical Corporation
1 devices