Data / Medical devices / United States / MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx
MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx: FDA-registered device maker in Carlsbad, CA, United States, 3 510(k) clearances
MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx is registered with the FDA (registration 2032809) in Carlsbad, CA, United States. It lists 8 device types. The FDA files 3 510(k) clearances under its listings, the newest dated March 16, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2032809
- FEI number
- 3004169154
- Address
- 6352 Corte Del Abeto Ste A, Carlsbad, CA, United States, 92011
- Owner or operator
- MILLENNIUM MEDICAL TECHNOLOGIES INC./DBA Cellmyx (9057868)
- Roles
- Manufacturer, Specification developer
- First device listed
- January 9, 2009
- Registered through
- 2026
- Brand names listed
- AcquiCell Pro, Aspiration tubing, Fat Collection and Transfer Cannisters and Lids, Fat Gun, Infiltration Cannulas, Infiltration tubing, Instrument Sleeve, IntelliFat and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Catheter | KGZ | 1 | Manufacturer | accessdata.fda.gov |
| Brush, Dermabrasion, Powered | GFE | 1 | Specification developer | accessdata.fda.gov |
| Cannula, Surgical, General & Plastic Surgery | GEA | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Manual, Surgical, General Use | MDM | 1 | Manufacturer | accessdata.fda.gov |
| Motor, Surgical Instrument, Ac-Powered | GEY | 1 | Manufacturer | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Manufacturer | accessdata.fda.gov |
| System, Suction, Lipoplasty | MUU | 2 | Manufacturer | accessdata.fda.gov |
| System, Suction, Lipoplasty For Removal | QPB | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 16, 2022 | K210528 | IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) Kit | MUU | Substantially Equivalent | Millennium Medical Technologies Inc (Dba Cellmyx) | accessdata.fda.gov |
| March 31, 2017 | K170449 | Autoclavable Suction Jar with Luer Lock extension - 250, 500, 1,000, 2,000 and 3,000 ml, Autoclavable Suction Jar without Luer Lock extension - 1,500 and 2,500 ml, Sterile 1,500 and 2,500 Lids with Conical patient connection 6-10 and overflow protection | MUU | Substantially Equivalent | Millennium Medical Technologies, Inc. | accessdata.fda.gov |
| July 10, 2008 | K081039 | LIPO CANNULA | QPB | Substantially Equivalent | Millennium Medical Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Syringe, Irrigating (Non Dental)
- All makers of System, Suction, Lipoplasty For Removal
- All makers of System, Suction, Lipoplasty
- All makers of Brush, Dermabrasion, Powered
- All makers of Accessories, Catheter
- All makers of Motor, Surgical Instrument, Ac-Powered
Updated March 16, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.