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 15, 2026, FDA's public records list Marco Ophthalmic, Inc. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Jul 27, 1994: MS-30 AUTOMATIC PERIMETER.
| Jul 27, 1994 | MS-30 AUTOMATIC PERIMETERK943234 · HPT | 510(k) clearances |
| Aug 9, 1993 | MARCO GXX SERIES PHOTOGRAPHIC SLIT LAMPSK930442 · HKI | 510(k) clearances |
| Aug 9, 1993 | MARCO STANDARD RADIUSGAUGESK930437 · HLF | 510(k) clearances |
| Aug 9, 1993 | MARCO STANDARD KERATOMETERSK930444 · HJB | 510(k) clearances |
| Aug 9, 1993 | MARCO MODELS G,H AND PRIMARY CARE SLIT LAMPSK930438 · HJO | 510(k) clearances |
| Jul 22, 1993 | MARCO SURGISCOPE OPERATION MICROSCOPESK930439 · HRM | 510(k) clearances |
| Jul 6, 1993 | MARCO INTERNATIONAL STANDK930440 · HMF | 510(k) clearances |
| Jul 6, 1993 | MARCO H AND TS-1 INSTRUMENT TABLESK930447 · HRJ | 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
