Humi Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Humi Corp. makes
Humi Corp. manufactures uterine manipulators and injectors, including a 4.5mm uterine manipulator and a 4.0mm uterine injector, designed for gynecological procedures.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Uterine Manipulator 4.5mm Ref K841681
Regimes: 510(k) Registry: 510(k)Uterine Injector 4.0mm Ref K841682
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Humi Corp. have in the registry?
The registry currently lists 2 devices for Humi Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Humi Corp.'s devices?
Among its 2 most recently registered devices, Humi Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Humi Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Humi Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Humi Corp. in the registry?
The most recently registered devices listed for Humi Corp. include UTERINE MANIPULATOR 4.5MM and UTERINE INJECTOR 4.0MM.