WeMED Bio-Tech, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
What WeMED Bio-Tech, Inc. makes
WeMED Bio-Tech, Inc. manufactures an intra medullary endo-transilluminating device (iMET device), designed for internal illumination within bone shafts during surgical procedures.
The company’s portfolio is regulated under Class II devices in the US, with the intra medullary endo-transilluminating device authorised via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does WeMED Bio-Tech, Inc. have in the registry?
The registry currently lists 1 device for WeMED Bio-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list WeMED Bio-Tech, Inc.'s devices?
Among its 1 most recently registered device, WeMED Bio-Tech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do WeMED Bio-Tech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for WeMED Bio-Tech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from WeMED Bio-Tech, Inc. in the registry?
The most recently registered devices listed for WeMED Bio-Tech, Inc. include Intra medullary endo-transilluminating device (iMET device).