Regenesis Biomedical, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K223620 | Reprieve by RegenesisTM | May 24, 2023 |
| K131979 | PROVANT THERAPY SYSTEM | December 13, 2013 |
| K091791 | PROVANT SYSTEM, MODEL 4201 | April 7, 2010 |
| K972093 | REGENESIS MODEL 42 | October 21, 1997 |