Orthodent Laboratory, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthodent Laboratory, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Vivid Aligners
1
Total
1
Cleared
0
Denied
Orthodent Laboratory, Inc. has 1 FDA 510(k) cleared medical devices. Based in Buffalo, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Orthodent Laboratory, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Compliance Systems International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Orthodent Laboratory, Inc.
1 devices