Alliance Global
TaiwanFDA applicant, unverified
- Devices
- 1
What Alliance Global makes
Alliance Global manufactures the Anker Dental Implant System, a dental implant solution designed for osseointegration in the jawbone to support dental prosthetics.
The Anker Dental Implant System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Anker Dental Implant System Ref K131165
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alliance Global have in the registry?
The registry currently lists 1 device for Alliance Global. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alliance Global's devices?
Among its 1 most recently registered device, Alliance Global has devices listed in FDA 510(k) (1 device).
What risk classes do Alliance Global's devices fall under?
Among its 1 most recently registered device, the classes recorded for Alliance Global's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alliance Global in the registry?
The most recently registered devices listed for Alliance Global include ANKER DENTAL IMPLANT SYSTEM.