Maihub Corp.
South KoreaFDA applicant, unverified FDA FEI 3043532712
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Maihub Corp. makes
Maihub Corp. manufactures the maiLink, a medical device designed for wireless connectivity in healthcare settings, enabling data transmission between devices and systems.
The maiLink 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
Company details
- FDA FEI number
- 3043532712
- DUNS number
- 987646067
- Address
- #503, 5F, 124 Teheran-ro, Gangnam-gu Seoul
- [email protected]
- Phone
- +82269491867
Frequently asked questions
How many devices does Maihub Corp. have in the registry?
The registry currently lists 2 devices for Maihub Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Maihub Corp.'s devices?
Among its 2 most recently registered devices, Maihub Corp. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Maihub Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Maihub Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Maihub Corp. in the registry?
The most recently registered devices listed for Maihub Corp. include maiLink.