Everlife Medical Equipment Co., Ltd.
TaiwanFDA applicant, unverified FDA FEI 3004753827
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Everlife Medical Equipment Co., Ltd. makes
Everlife Medical Equipment Co., Ltd. makes transcutaneous muscle stimulators and powered muscle stimulators, including models E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, and E-201311. The company also makes interferential current therapy devices, such as model IF-100507.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Everelife Transcutaneous Muscle Stimulator Ref K071624
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004753827
- Address
- 8F, No. 8, Lane 235, New Taipei City
Frequently asked questions
How many devices does Everlife Medical Equipment Co., Ltd. have in the registry?
The registry currently lists 3 devices for Everlife Medical Equipment Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Everlife Medical Equipment Co., Ltd.'s devices?
Among its 3 most recently registered devices, Everlife Medical Equipment Co., Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Everlife Medical Equipment Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Everlife Medical Equipment Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Everlife Medical Equipment Co., Ltd. in the registry?
The most recently registered devices listed for Everlife Medical Equipment Co., Ltd. include EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR, EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211, E-201311 and EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507.