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 15, 2026, FDA's public records list FCI Ophthalmics with 13 510(k) clearances. The most recent is a 510(k) clearance dated Aug 7, 2006: MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE.
| Aug 7, 2006 | MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICEK061404 · OKS | 510(k) clearances |
| Jul 11, 2006 | SNUG PLUG PUNCTUM PLUGK061398 · LZU | 510(k) clearances |
| Nov 18, 2004 | SELF RETAINING BICANALICULUS INTUBATION SETK041869 · OKS | 510(k) clearances |
| Sep 17, 2003 | BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)K023758 · OKS | 510(k) clearances |
| Aug 22, 2003 | FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANTK023400 · HPZ | 510(k) clearances |
| Feb 26, 2003 | DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSESK030054 · HJK | 510(k) clearances |
| Apr 19, 2000 | BIOCERAMIC ORBITAL IMPLANTK992294 · HPZ | 510(k) clearances |
| Jul 8, 1999 | FCI CRAWFORD PROBE INTUBATION SETSK991238 · OKS | 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
