# Stryker GI

- Location (FDA's records): Flower Mound, TX
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: FDF (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (0 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
- Sightline Technologies, Ltd.: 1 (https://510kreport.com/company/sightline-technologies)

## Firms that cite its devices most
- Sheathing Technologies, Inc.: 1 (https://510kreport.com/company/sheathing-technologies)
- Peermedical, Ltd.: 1 (https://510kreport.com/company/peermedical)

## Its most-cited devices
- K081004: Protectiscope CS Colonoscope, Non-Intrapull (2008), cited by 2

## Recent decisions
- K081004: Protectiscope CS Colonoscope, Non-Intrapull (May 2, 2008)

Source page: https://510kreport.com/company/stryker-gi