Diamond Orthotic Laboratory is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diamond Orthotic Laboratory - FDA 510(k) Cleared Devices
Recent clearances: Diamond Digital Sleep Orthotic (DDSO)
1
Total
1
Cleared
0
Denied
Diamond Orthotic Laboratory has 1 FDA 510(k) cleared medical devices. Based in La Mesa, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Diamond Orthotic Laboratory Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Diamond Orthotic Laboratory
1 devices