# Integrated Endoscopy, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 3 (2014–2025): 3 510(k) clearances
- Product codes: HRX (2), GCJ (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Lazurite Holdings, LLC: 1 (https://510kreport.com/company/lazurite-holdings)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)

## Firms that cite its devices most
- Prosurg, Inc.: 1 (https://510kreport.com/company/prosurg)

## Its most-cited devices
- K140903: Nuvis Arthroscope (2014), cited by 2

## Recent decisions
- K242606: Nuvis® Wireless HD Camera System (Nuvis-2K) (Nov 20, 2025)
- K191594: Nuvis Battery Arthroscope (Jul 11, 2019)
- K140903: Nuvis Arthroscope (Jul 17, 2014)

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