Bodycad Laboratories, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 16
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K253300 | Fine Osteotomy | October 28, 2025 |
| K250394 | Fine TTO | October 21, 2025 |
| K250923 | Fine Osteotomy | August 21, 2025 |
| K241356 | Fine Osteotomy | September 5, 2024 |
| K240703 | Fine Osteotomy | April 12, 2024 |
| K240066 | Fine Osteotomy | February 9, 2024 |
| K231314 | Fine Osteotomy | June 2, 2023 |
| K212307 | BC Reflex Uni Knee System | October 12, 2021 |
| K211895 | BC Reflex Uni Knee System | August 20, 2021 |
| K211646 | FINE Osteotomy | July 28, 2021 |
| K203697 | BC Reflex Uni Knee System | March 12, 2021 |
| K193614 | FINE Osteotomy around the knee | March 25, 2020 |
| K191996 | BC Reflex Uni Knee System | December 5, 2019 |
| K191150 | Bodycad Unicompartmental Knee System | October 8, 2019 |
| K181302 | Bodycad Unicompartmental Knee System | January 17, 2019 |
| K163700 | Bodycad Unicompartmental Knee System | March 29, 2017 |