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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Ocular Instruments with 50 510(k) clearances. The most recent is a 510(k) clearance dated Mar 4, 2002: STAURENGHI WIDE FIELD SCANNING LASER LENS.
| Date | Record | Source |
|---|---|---|
| Mar 4, 2002 | STAURENGHI WIDE FIELD SCANNING LASER LENSK014170 · HJK | 510(k) clearances |
| Aug 24, 2001 | DISPOSABLE VITRECTOMY LENSK012096 · HJK | 510(k) clearances |
| Nov 8, 1994 | MANDELKORN SUTURE LYSIS LENSK933976 · HJK | 510(k) clearances |
| Oct 31, 1994 | RITCH NYLON SUTURE LASER LENSK933264 · HJK | 510(k) clearances |
| Aug 29, 1994 | 50 DEGREE HRI PRISM LENSK941420 · HJK | 510(k) clearances |
| Apr 1, 1994 | OSHER SURGICAL GONIO/POSTERIOR POLE LENSK935302 · HKS | 510(k) clearances |
| Nov 16, 1992 | BYRNE EXPULSIVE LENSK923670 · HJI | 510(k) clearances |
| Nov 16, 1992 | TROKEL /3 GONIO LASER LENSK921414 · LQJ | 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
