Megagen Co., Ltd.
Country not established
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Rescue Implant System Ref K053353
Regimes: 510(k) Registry: 510(k)Rescue Internal Implant System Ref K073058
Regimes: 510(k) Registry: 510(k)Intermezzo Plus Fixture Ref K053354
Regimes: 510(k) Registry: 510(k)Rescue Internal Implant System Ref K063216
Regimes: 510(k) Registry: 510(k)Exfeel Implant System Ref K052369
Regimes: 510(k) Registry: 510(k)Ez Plus Implant System Ref K070562
Regimes: 510(k) Registry: 510(k)Anyridge Internal Implant System Ref K110955
Regimes: 510(k) Registry: 510(k)Ball Abutment System Ref K101890
Regimes: 510(k) Registry: 510(k)Intermezzo Implant Systems Ref K051018
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Megagen Co., Ltd. have in the registry?
The registry currently lists 9 devices for Megagen Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Megagen Co., Ltd.'s devices?
Among its 9 most recently registered devices, Megagen Co., Ltd. has devices listed in FDA 510(k) (9 devices).
What risk classes do Megagen Co., Ltd.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Megagen Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Megagen Co., Ltd. in the registry?
The most recently registered devices listed for Megagen Co., Ltd. include RESCUE IMPLANT SYSTEM, RESCUE INTERNAL IMPLANT SYSTEM, INTERMEZZO PLUS FIXTURE and EXFEEL IMPLANT SYSTEM.