Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled 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 Keeler Optical Products, Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 13, 1981: KEELER/KONAN SPECULAR MICROSCOPE.
| May 13, 1981 | KEELER/KONAN SPECULAR MICROSCOPEK810403 · HJO | 510(k) clearances |
| Jul 21, 1980 | KEELER AMOILS ACULL CRYO OPHTHALMIC UNITK801418 · HPS | 510(k) clearances |
| Dec 11, 1979 | NEVYAS AUTOPRESS EYE COMPRESSORK792255 · LCC | 510(k) clearances |
| Jan 26, 1979 | LEVIGATOR, KEELER PHOKOK782141 · HQC | 510(k) clearances |
| Dec 4, 1978 | LOCATOR, FOREIGN BODYK781892 · HPM | 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
