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 American Endoscopy with 19 510(k) clearances. The most recent is a 510(k) clearance dated Oct 17, 1985: AMERICAN DILATATION SYSTEM.
| Oct 17, 1985 | AMERICAN DILATATION SYSTEMK853274 · KNQ | 510(k) clearances |
| Jul 19, 1984 | PROXIMA 1 PH MONITORK841384 · FFT | 510(k) clearances |
| Apr 25, 1984 | ENDO BITE BLOCKK833491 · KTI | 510(k) clearances |
| Apr 13, 1984 | BIOPSY FORCEPSK840818 · FCL | 510(k) clearances |
| Jan 3, 1984 | TAMPONADE BALLOON CUFFK833859 · GCP | 510(k) clearances |
| Nov 29, 1983 | PERCUTANEOUS ENDOSCOPIC GASTROSCOPYK833492 · KNT | 510(k) clearances |
| Oct 20, 1983 | AUTOMATIC ENDOSCOPEK832458 · NVE | 510(k) clearances |
| Sep 24, 1982 | RETRIEVAL BALLOONSK821818 · KOD | 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
