Terray Corp.
CanadaFDA applicant, unverified
- Devices
- 4
What Terray Corp. makes
Terray Corp. manufactures orthopedic fixation devices, including stainless steel rods for surgical applications, resurfacing joint implants in small, medium, and large sizes, and wrist fusion plates. Their product line also covers distal clavicular immobilization plates for left and right shoulders, designed to stabilize bone fragments during healing.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. These products are intended for use in the United States, where they are subject to compliance with FDA requirements for orthopedic implants and fixation hardware.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Carpal Engaging Wrist Fusion Plate Ref K974030
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Terray Corp. have in the registry?
The registry currently lists 4 devices for Terray Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Terray Corp.'s devices?
Among its 4 most recently registered devices, Terray Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Terray Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Terray Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Terray Corp. in the registry?
The most recently registered devices listed for Terray Corp. include TERRAY STAINLESS STEEL ROD (STRAIGHT, L, RECTANGLE), MTP RESESURFACING JOINT-SMALL/9301-01; MEDIUM/9301-02; LARGE/9301-03, CARPAL ENGAGING WRIST FUSION PLATE and DISTAL CLAVICULAR FRAGMENT IMMOBILIZATION PLATE LEFT, MODEL 1810-116_126-03 (05, 07) RIGHT 1811-116_126-03 (05, 07).