Gergens Orthodontic Lab is one of 22384 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gergens Orthodontic Lab - FDA 510(k) Cleared Devices
Recent clearances: Dorsal Appliance, ACRYLIC HERBST APPLIANCE
2
Total
2
Cleared
0
Denied
Gergens Orthodontic Lab has 2 FDA 510(k) cleared medical devices. Based in Dunlap, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Gergens Orthodontic Lab Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Backroads Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Gergens Orthodontic Lab
2 devices