Techheim Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Techheim Co., Ltd. makes
Techheim Co., Ltd. manufactures the NubeX, a medical device designed for [specific application not detailed in provided data].
The NubeX is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
NubeX Ref K211480
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Techheim Co., Ltd. have in the registry?
The registry currently lists 1 device for Techheim Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Techheim Co., Ltd.'s devices?
Among its 1 most recently registered device, Techheim Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Techheim Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Techheim Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Techheim Co., Ltd. in the registry?
The most recently registered devices listed for Techheim Co., Ltd. include NubeX.