Glidewell Laboratories is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Glidewell Laboratories - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Glidewell Laboratories has 3 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Historical record: 3 cleared submissions from 1997 to 2006. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Glidewell Laboratories Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Glidewell Laboratories
3 devices