Orthoselect, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthoselect, LLC - FDA 510(k) Cleared Devices
Recent clearances: DIBS (Digital Indirect Bonding System)
1
Total
1
Cleared
0
Denied
Orthoselect, LLC has 1 FDA 510(k) cleared medical devices. Based in American Fork, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Orthoselect, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emma International Consulting Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Orthoselect, LLC
1 devices