# Arrinex, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 3 (2016–2019): 3 510(k) clearances
- Product codes: GEH (3)
- 510(k) review time since 2016: median 107 days, against 83 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 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
- H&O Equipments, Nv/Sa: 1 (https://510kreport.com/company/h-o-equipments)

## Its most-cited devices
- K160669: ClariFix Device (2016), cited by 1
- K162608: ClariFix Device (2017), cited by 1

## Recent decisions
- K190356: ClariFix (Feb 26, 2019)
- K162608: ClariFix Device (Feb 14, 2017)
- K160669: ClariFix Device (Jun 24, 2016)

Source page: https://510kreport.com/company/arrinex