Mentor Corporation - FDA 510(k) Cleared Devices
Recent clearances: MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER, MENTOR ARIS SUPRAPUBIC SURGICAL KIT, MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETER
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mentor Corporation Gastroenterology & Urology ✕
3 devices