Everlife Medical Instrument Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Everlife Medical Instrument Co., Ltd. makes
Everlife Medical Instrument Co., Ltd. manufactures medical devices under the EVERLIFE brand, including Class II devices such as surgical instruments and related accessories designed for procedural applications.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices and is listed in the FDA 510(k) registry. The manufacturer is based in the United States.
Catalogue
Everlife Ref K050788
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Everlife Medical Instrument Co., Ltd. have in the registry?
The registry currently lists 1 device for Everlife Medical Instrument Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Everlife Medical Instrument Co., Ltd.'s devices?
Among its 1 most recently registered device, Everlife Medical Instrument Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Everlife Medical Instrument Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Everlife Medical Instrument Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Everlife Medical Instrument Co., Ltd. in the registry?
The most recently registered devices listed for Everlife Medical Instrument Co., Ltd. include EVERLIFE.