Mentor Ophthalmics, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K973146 | MENTOR SUPER ABSORBENT DRAPE | December 4, 1997 |
| K971538 | MENTOR GEMINI HEMOSTATIC ERASER | July 14, 1997 |
| K964312 | MENTOR TONO-PEN 3 | November 26, 1996 |
| K960765 | MENTOR ADVENT A/B SYSTEM | August 8, 1996 |