# Global Endoscopy, Inc.

- Location (FDA's records): Schaumburg, IL
- FDA decisions: 7 (2001–2001): 7 510(k) clearances
- Product codes: HRX (1), FGB (1), EOB (1), GCJ (1), FAJ (1), HIH (1), HET (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K003802: Hysteroscopes (Jul 22, 2001)
- K003805: Gynecological Laparoscopes (Jul 22, 2001)
- K003831: Arthroscopes (Jul 20, 2001)
- K003830: Ent Endoscopes (Apr 9, 2001)
- K003803: General Surgical Laparoscopes (Mar 7, 2001)
- K003806: Ureteroscopes (Feb 22, 2001)
- K003807: Cystoscopes (Feb 22, 2001)

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