Biovalve Technologies, Inc. is one of 25355 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biovalve Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIOVALVE MINI-JECT NEEDLEFREE INJECTOR, BIOVALVE INSULIN DELIVERY SYSTEMS (BIDS), BIOVALVE MINIJECT NEEDLE-FREE INJECTION SYSTEM, MODEL FG-01-001
3
Total
3
Cleared
0
Denied
Biovalve Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Worcester, US.
Historical record: 3 cleared submissions from 2004 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Biovalve Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biovalve Technologies, Inc.
3 devices