Mli Mli Group Inc
United Statesfrom the FDA registration address FDA establishment FEI 3039199439
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Mli Mli Group Inc makes
MLI MLI GROUP INC manufactures tinted non-prescription spectacles designed for general eyewear use, including options for UV protection and color correction.
These products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
- Registry: GUDID
Company details
- FDA FEI number
- 3039199439
- Address
- 4553 Glencoe Avenue Suite 230, Marina del Rey, CA, 90292
Frequently asked questions
How many devices does MLI MLI GROUP INC have in the registry?
The registry currently lists 1 device for MLI MLI GROUP INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list MLI MLI GROUP INC's devices?
Among its 1 most recently registered device, MLI MLI GROUP INC has devices listed in FDA GUDID (1 device).
What risk classes do MLI MLI GROUP INC's devices fall under?
Among its 1 most recently registered device, the classes recorded for MLI MLI GROUP INC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from MLI MLI GROUP INC in the registry?
The most recently registered devices listed for MLI MLI GROUP INC include MLi MLi Timeless.