Mmi, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Mmi, Inc. makes
Mmi, Inc. manufactures single-use surgical gloves under the DUAL FLEX NON-LATEX brand, designed for medical and procedural applications requiring latex-free protection. The company also produces G.I. cleansing kits, intended for gastrointestinal preparation and patient hygiene, as well as the CLAMP-N-CUT device, a surgical tool for tissue manipulation and cutting during procedures.
The company’s portfolio includes devices classified under Class I and Class II regulatory categories, with several products authorised via the FDA’s 510(k) clearance process. These products are listed in the FDA’s regulatory database, and the manufacturer operates from the United States.
Catalogue
Dual Flex Non-Latex Ref K905026
Regimes: 510(k) Registry: 510(k)G.I. Cleansing Kit Ref K842130
Regimes: 510(k) Registry: 510(k)Clamp-N-Cut Ref K860445
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mmi, Inc. have in the registry?
The registry currently lists 3 devices for Mmi, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mmi, Inc.'s devices?
Among its 3 most recently registered devices, Mmi, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mmi, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mmi, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mmi, Inc. in the registry?
The most recently registered devices listed for Mmi, Inc. include DUAL FLEX NON-LATEX, G.I. CLEANSING KIT and CLAMP-N-CUT.