Mend Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K924094 | MEND APC | March 30, 1993 |
| K883867 | CERVICAL BIOPSY INSTRUMENT | November 29, 1988 |
| K884558 | IOP ADJUSTABLE STIRRUP | November 17, 1988 |