Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Johnson & JohnsonLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 14, 2026, FDA's public records list Mentor Corporation with 65 510(k) clearances. The most recent is a 510(k) clearance dated Apr 11, 2013: MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXP….
| Apr 11, 2013 | MENTOR CPX 4 BREAST TISSUE EXPANDERS AND MENTOR CPX 4 WITH SUTURE TABS BREAST TISSUE EXPANDERSK130813 · LCJ | 510(k) clearances |
| Oct 10, 2006 | MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZERK062421 · MRD | 510(k) clearances |
| Dec 27, 2005 | MENTOR NOVASILK MESHK053414 · OTP | 510(k) clearances |
| Dec 15, 2005 | MENTOR ARIS SUPRAPUBIC SURGICAL KITK053296 · OTN | 510(k) clearances |
| Oct 11, 2005 | MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETERK052440 · EZD | 510(k) clearances |
| Jun 3, 2005 | MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETERK050008 · EZD | 510(k) clearances |
| Mar 9, 2005 | MENTOR ARIS TRANS-OBTURATOR TAPE AND SURGICAL KITK050148 · OTN | 510(k) clearances |
| Nov 9, 2004 | MENTOR OBTAPE TRANS-OBTURATOR SURGICAL KITK042851 · OTN | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built