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 Cortek Endoscopy, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 13, 2000: CORTEK MINI LAPAROSCOPE.
| Apr 13, 2000 | CORTEK MINI LAPAROSCOPEK000199 · HET | 510(k) clearances |
| Apr 11, 2000 | CORTEK ARTHROSCOPEK000198 · HRX | 510(k) clearances |
| Mar 31, 2000 | CORTEK LAPAROSCOPESK000202 · GCJ | 510(k) clearances |
| Mar 3, 2000 | CORTEK URETHEROSCOPEK000200 · FGB | 510(k) clearances |
| Mar 3, 2000 | CORTEK CYSTOSCOPEK000197 · FAJ | 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
