Medical Device Manufacturer · US , South Plainfield , NJ

Unipack, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

Unipack, LLC has 1 FDA 510(k) cleared medical devices. Based in South Plainfield, US.

Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Unipack, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Unipack, LLC

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