Orthoaccel Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K153048 | AcceleDent Aura | July 8, 2016 |
| K130643 | ACCELEDENT AURA | April 23, 2013 |
| K110661 | ACCELEDENT | November 17, 2011 |