Hdt Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Hdt Co., Ltd. makes
Hdt Co., Ltd. manufactures the Mine ALNU (Model: Mine 2.1), a medical device designed for [specific clinical application not detailed in provided data]. This product is intended for [purpose not specified in data], adhering to regulatory standards for its intended use.
The Mine ALNU (Model: Mine 2.1) falls under Class II classification in the US and is listed in the FDA’s 510(k) registry. The company is based in the United States, where its devices are subject to FDA oversight.
Catalogue
MINE ALNU (Model: Mine 2.1) Ref K213405
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hdt Co., Ltd. have in the registry?
The registry currently lists 1 device for Hdt Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hdt Co., Ltd.'s devices?
Among its 1 most recently registered device, Hdt Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Hdt Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hdt Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hdt Co., Ltd. in the registry?
The most recently registered devices listed for Hdt Co., Ltd. include MINE ALNU (Model: Mine 2.1).