The O R Company Pty, Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K220202 | Uterine ElevatOR PRO with OccludOR Balloon | March 31, 2022 |
| K212505 | DUMI ManipulatOR | January 10, 2022 |