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 13, 2026, FDA's public records list Cilco, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated May 2, 1986: CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGE.
| Date | Record | Source |
|---|---|---|
| May 2, 1986 | CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGEK861334 · HNN | 510(k) clearances |
| Feb 27, 1986 | CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)K854969 · IYO | 510(k) clearances |
| Apr 30, 1985 | K-SOLK844249 · LYX | 510(k) clearances |
| Feb 14, 1985 | CILCO I/A SURGICAL PACKK843319 · HQC | 510(k) clearances |
| Nov 21, 1984 | CILCOR OPHTHALMIC INSTRUMENTSK843992 · HNR | 510(k) clearances |
| Oct 5, 1984 | CILCO DIAMOND KNIFEK843447 · HNN | 510(k) clearances |
| Jun 19, 1984 | OCTOPUS 500/500EK841099 · HPT | 510(k) clearances |
| Apr 5, 1984 | CYSTOTOME, 140-SK840475 · HNY | 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
