# United State Endoscopy Group, Inc.

- Location (FDA's records): Mentor, OH
- FDA decisions: 1 (2017–2017): 1 510(k) clearance
- Product codes: FEQ (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
- K163424: AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON (Jan 4, 2017)

Source page: https://510kreport.com/company/united-state-endoscopy-group