# American Endoscopy, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 19 (1982–1985): 19 510(k) clearances
- Product codes: FGE (2), KNS (2), KOD (2), KNQ (1), KTI (1), FCL (1), NVE (1), OCZ (1), ODD (1), GEI (1), GEE (1), GCP (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Conmed Corporation: 1 (https://510kreport.com/company/conmed)
- Conmed Endoscopic Technologies, Inc.: 1 (https://510kreport.com/company/conmed-endoscopic-technologies)

## Its most-cited devices
- K820430: Diathermic Snares (1982), cited by 2

## Recent decisions
- K853274: American Dilatation System (Oct 17, 1985)
- K841384: Proxima 1 PH Monitor (Jul 19, 1984)
- K833491: Endo Bite Block (Apr 25, 1984)
- K840818: Biopsy Forceps (Apr 13, 1984)
- K833859: Tamponade Balloon Cuff (Jan 3, 1984)
- K833492: Percutaneous Endoscopic Gastroscopy (Nov 29, 1983)
- K832458: Automatic Endoscope (Oct 20, 1983)
- K821818: Retrieval Balloons (Sep 24, 1982)

Source page: https://510kreport.com/company/american-endoscopy