Medical device makerLabelled 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.
As of Nov 14, 2026, FDA's public records list Optik with 6 510(k) clearances. The most recent is a 510(k) clearance dated Mar 16, 1994: OPTIK LAPAROSCOPE.
| Mar 16, 1994 | OPTIK LAPAROSCOPEK933776 · GCJ | 510(k) clearances |
| Jun 1, 1993 | COAST VIDEO ENDOSCOPIC IMAGING SYSTEMK926166 · FWF | 510(k) clearances |
| Apr 16, 1990 | TITAMED ANTWERP SYSTEMK896404 · JEY | 510(k) clearances |
| Dec 27, 1989 | MANUAL SURGICAL INSTRUMENTS FOR TITAMED ANTWERPK896589 · LRZ | 510(k) clearances |
| Aug 7, 1989 | LIGHTSCOPE SETK894557 · HRW | 510(k) clearances |
| Aug 7, 1989 | MINI LIGHTSCOPE SET, LIGHTSCOPE JR. SETK894558 · HRX | 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
