Medical Device Manufacturer · US , Great Neck , NY

Bionime Corporation - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 2005
21
Total
21
Cleared
0
Denied

Bionime Corporation has 21 FDA 510(k) cleared chemistry devices. Based in Great Neck, US.

Latest FDA clearance: Nov 2024. Active since 2005.

Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Dynamic Biotech, Inc. Dba. Ivdd Regulatory Consultant and Symbiosis Consulting , Ltd..

FDA 510(k) Regulatory Record - Bionime Corporation
21 devices
1-12 of 21
Filters