VPro5
510(k) K183018
VPro5 is a medical device (FDA Class II; FDA product code OYH, Orthodontic Vibratory Accessory) made by Propel Orthodontics LLC, cleared under FDA 510(k) K183018 on 1 Nov 2019, active as of 11 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK183018 | Date1 Nov 2019 | StatusActive |
Official records
- FDA 510(k) database K183018
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- OYH
- FDA applicant
- Propel Orthodontics, LLC
- Device class
- Class II
- Regulation
- 21 CFR Part 872.5470
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code OYH (Orthodontic Vibratory Accessory).