Ordont Orthodontic Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ordont Orthodontic Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SmileSeries
1
Total
1
Cleared
0
Denied
Ordont Orthodontic Laboratories, Inc. has 1 FDA 510(k) cleared medical devices. Based in Fenton, US.
Last cleared in 2022. Active since 2022. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ordont Orthodontic Laboratories, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Trisler Consulting, Dba as regulatory consultant.
FDA 510(k) Regulatory Record - Ordont Orthodontic Laboratories, Inc.
1 devices