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 14, 2026, FDA's public records list Miami Eye Technology, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 16, 1984: CLAYMAN-PAREL CAPSULE COUPEUR.
| May 16, 1984 | CLAYMAN-PAREL CAPSULE COUPEURK841101 · HNY | 510(k) clearances |
| Jan 10, 1984 | GELENDER VACUUM FIXATION RING SYSK832912 · HNH | 510(k) clearances |
| Nov 28, 1983 | SURGICAL IOP MONITORK832996 · HKY | 510(k) clearances |
| Oct 4, 1983 | EPA AUTOMATED INFUSION POLEK832997 · HQC | 510(k) clearances |
| Sep 29, 1983 | ABBOTT GLOBE HOLDERK832911 · HJO | 510(k) clearances |
| Jun 30, 1983 | RARE-EARTH INTRA-OCULAR MAGNETK831702 · HPN | 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
