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MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx

United Statesfrom the FDA registration address FDA establishment FEI 3004169154

Devices
1
Registrations
FDA
FDA recalls
0

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3004169154
Address
6352 Corte Del Abeto Ste A, Carlsbad, CA, 92011

Frequently asked questions

How many devices does MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx have in the registry?

The registry currently lists 1 device for MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx. Devices recorded under merged duplicate company entries are counted once.

Which registries list MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx's devices?

Among its 1 most recently registered device, MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx has devices listed in FDA 510(k) (1 device).

What risk classes do MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx's devices fall under?

Among its 1 most recently registered device, the classes recorded for MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx in the registry?

The most recently registered devices listed for MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx include IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.