Propel Orthodontics, LLC is one of 13015 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Propel Orthodontics, LLC - FDA 510(k) Cleared Devices
Recent clearances: VPro5, PROPEL Device, PROPEL device
3
Total
3
Cleared
0
Denied
Propel Orthodontics, LLC has 3 FDA 510(k) cleared medical devices. Based in Milpitas, US.
Historical record: 3 cleared submissions from 2015 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Propel Orthodontics, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Coombs Medical Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Propel Orthodontics, LLC
3 devices