# Valley Contax, Inc.

- Location (FDA's records): Springfield, OR
- FDA decisions: 3 (2017–2022): 3 510(k) clearances
- Product codes: HQD (3)
- 510(k) review time since 2016: median 50 days, against 66 for FDA's reviews in the same codes and years (2 of 3 faster)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (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
- Contamac, Ltd.: 4 (https://510kreport.com/company/contamac)
- Bostonsight: 1 (https://510kreport.com/company/bostonsight)

## Its most-cited devices
- K170335: Custom Stable (TM) Rigid Gas Permeable Scleral Contact Lens (2017), cited by 1

## Recent decisions
- K213880: Custom Stable Rigid Gas Permeable Scleral Contact Lens (Jan 7, 2022)
- K202860: Valley Contax Single Vision (SV) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax Goldeneye Aspheric Front Multifocal (AFM) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A), Valley Contax V Kone (VK) Gas Permeable Contact Lens (roflufocon D, roflufocon E, tisilfocon A, hexafocon A, enflufocon A) (May 11, 2021)
- K170335: Custom Stable (TM) Rigid Gas Permeable Scleral Contact Lens (Mar 24, 2017)

Source page: https://510kreport.com/company/valley-contax