# Terray Corp.

- Location (FDA's records): Arnprior, CA
- FDA decisions: 4 (1998–2007): 4 510(k) clearances
- Product codes: HRS (2), KWD (1), KWP (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
- K063275: Distal Clavicular Fragment Immobilization Plate Left, Model 1810-116_126-03 (05,07) Right 1811-116_126-03 (05,07) (Jul 27, 2007)
- K003911: Terray Stainless Steel Rod (Straight, L, Rectangle) (Mar 13, 2001)
- K003629: MTP Resesurfacing Joint-Small/9301-01; Medium/9301-02; Large/9301-03 (Feb 22, 2001)
- K974030: Carpal Engaging Wrist Fusion Plate (Jan 21, 1998)

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