Alliance Global Technology Co., Ltd.
TaiwanFDA applicant, unverified FDA FEI 3009325911
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Alliance Global Technology Co., Ltd. makes
Alliance Global Technology Co., Ltd. manufactures dental implant systems, including the Anker Dental Implant System (SB-III, ST, and AT series) and the Anker II Dental Implant System. These products are designed for dental professionals to place and secure dental implants in patients requiring tooth replacement solutions.
The company’s dental implant systems are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Anker II Dental Implant System Ref K152576
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009325911
- Address
- 2F., No. 92 & 96, Luke 5th Rd., Kaohsiung Science Park, Luzhu Dist.,, Kaohsiung
Frequently asked questions
How many devices does Alliance Global Technology Co., Ltd. have in the registry?
The registry currently lists 2 devices for Alliance Global Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alliance Global Technology Co., Ltd.'s devices?
Among its 2 most recently registered devices, Alliance Global Technology Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Alliance Global Technology Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alliance Global Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alliance Global Technology Co., Ltd. in the registry?
The most recently registered devices listed for Alliance Global Technology Co., Ltd. include Anker Dental Implant System - SB-III, ST and AT series and Anker II Dental Implant System.