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 its name, each linked to the record. See the Johnson & Johnson group view.
As of Nov 15, 2026, FDA's public records list Mitek Surgical Products, Inc. with 31 510(k) clearances. The most recent is a 510(k) clearance dated Jan 31, 1996: MITEK THREADED ANCHOR (FASTIN).
| Jan 31, 1996 | MITEK THREADED ANCHOR (FASTIN)K953560 · MBI | 510(k) clearances |
| Dec 29, 1995 | MITEK GII ANCHORK953877 · MBI | 510(k) clearances |
| Oct 31, 1995 | MITEK MINI ANCHORK936311 · MNV | 510(k) clearances |
| Oct 24, 1995 | MITEK ABSORBABLE ANCHORK941599 · MNV | 510(k) clearances |
| Aug 2, 1995 | ABSORBALBE ANCHORK944051 · MNV | 510(k) clearances |
| May 22, 1995 | MITEK TOGGLE ANCHOR(TM)K950070 · JDR | 510(k) clearances |
| Mar 24, 1995 | MITEK G III ANCHOR, MITEK LS ANCHORK944936 · JDR | 510(k) clearances |
| Mar 6, 1995 | MITEK THRADED ANCHOR (MTA)K945203 · JDR | 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
