Bacou USA, Inc. and Uvex Safety, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bacou USA, Inc. and Uvex Safety, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Bacou USA, Inc. and Uvex Safety, Inc. has 3 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 3 cleared submissions from 1982 to 1992. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Bacou USA, Inc. and Uvex Safety, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bacou USA, Inc. and Uvex Safety, Inc.
3 devices