T-Plus Implant Tech. Co., Ltd.
TaiwanFDA 510(k) applicant, unverified
- Devices
- 4
What T-Plus Implant Tech. Co., Ltd. makes
T-Plus Implant Tech. Co., Ltd. manufactures internal fixation systems for orthopedic applications, including the ST Internal Fixture System, TI STAR Implant System, and A Plus Internal Fixture System. These devices are designed for bone stabilization and fracture fixation, providing structural support during the healing process.
The company’s products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
ST Internal Fixture System Ref K152787
510(k) 510(k)Ti Star Implant System Ref K132992
510(k) 510(k)A Plus Internal Fixture System Ref K152786
510(k) 510(k)ST Internal Implant System Ref K190919
510(k) 510(k)
Frequently asked questions
How many devices does T-Plus Implant Tech. Co., Ltd. have in the registry?
The registry currently lists 4 devices for T-Plus Implant Tech. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list T-Plus Implant Tech. Co., Ltd.'s devices?
Among its 4 most recently registered devices, T-Plus Implant Tech. Co., Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do T-Plus Implant Tech. Co., Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for T-Plus Implant Tech. Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from T-Plus Implant Tech. Co., Ltd. in the registry?
The most recently registered devices listed for T-Plus Implant Tech. Co., Ltd. include ST Internal Fixture System, TI STAR IMPLANT SYSTEM, A Plus Internal Fixture System and ST Internal Implant System.