Millimax Corp.
South KoreaFDA applicant, unverified
- Devices
- 2
What Millimax Corp. makes
Millimax Corp. manufactures latex surgical gloves and patient examination gloves, designed for sterile and non-sterile medical procedures.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Latex Surgical Gloves Ref K892922
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves Ref K892921
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Millimax Corp. have in the registry?
The registry currently lists 2 devices for Millimax Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Millimax Corp.'s devices?
Among its 2 most recently registered devices, Millimax Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Millimax Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Millimax Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Millimax Corp. in the registry?
The most recently registered devices listed for Millimax Corp. include LATEX SURGICAL GLOVES and PATIENT EXAMINATION GLOVES.