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 Coburn Optical Industries with 14 510(k) clearances. The most recent is a 510(k) clearance dated May 26, 1989: MAGNILINK SYSTEM 209.
| May 26, 1989 | MAGNILINK SYSTEM 209K892349 · HJG | 510(k) clearances |
| May 26, 1989 | MAGNILINK SYSTEM 602K892351 · HJG | 510(k) clearances |
| May 26, 1989 | MAGNILINK SYSTEM 201K892348 · HJG | 510(k) clearances |
| May 26, 1989 | MAGNILINK SYSTEM 101K892347 · HJG | 510(k) clearances |
| May 26, 1989 | MAGNILINK SYSTEM 402/5K892350 · HJG | 510(k) clearances |
| Aug 21, 1986 | IRRIGATION & ASPIRATION/VITRECTOMY DEVICEK862188 · HQE | 510(k) clearances |
| Oct 15, 1985 | COBURN I/A SYSTEMK853457 · HQE | 510(k) clearances |
| Jul 2, 1982 | DISP. MICROSURGICAL KNIVESK821737 · GES | 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
