Mentor Corporation
Mentor Corporation appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 10, 2006.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K062421 | MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER | October 10, 2006 |
| K053296 | MENTOR ARIS SUPRAPUBIC SURGICAL KIT | December 15, 2005 |
| K052440 | MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETER | October 11, 2005 |
| K050148 | MENTOR ARIS TRANS-OBTURATOR TAPE AND SURGICAL KIT | March 9, 2005 |