Active Life Scientific, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K250216 | OsteoProbe (OP-100) | September 11, 2025 |
| K221195 | OsteoProbe | June 28, 2022 |
| DEN210013 | OsteoProbe | August 19, 2021 |