Aitewan Biomedical Technology, Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
What Aitewan Biomedical Technology, Inc. makes
Aitewan Biomedical Technology, Inc. manufactures the DeepBT Detector-Plus, a device designed for detecting specific biological signals or markers in medical imaging applications.
The DeepBT Detector-Plus is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
DeepBT Detector-Plus Ref K252190
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aitewan Biomedical Technology, Inc. have in the registry?
The registry currently lists 1 device for Aitewan Biomedical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aitewan Biomedical Technology, Inc.'s devices?
Among its 1 most recently registered device, Aitewan Biomedical Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aitewan Biomedical Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aitewan Biomedical Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aitewan Biomedical Technology, Inc. in the registry?
The most recently registered devices listed for Aitewan Biomedical Technology, Inc. include DeepBT Detector-Plus.