Data / Medical devices / United States / Millennium Dental Technologies, Inc.
Millennium Dental Technologies, Inc.: FDA-registered device maker in Cerritos, CA, United States, 3 510(k) clearances
Millennium Dental Technologies, Inc. is registered with the FDA (registration 2031763) in Cerritos, CA, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated July 12, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2031763
- FEI number
- 3002690217
- Address
- 10945 South ST., Suite 104-A, Cerritos, CA, United States, 90703
- Owner or operator
- MILLENNIUM DENTAL TECHNOLOGIES, INC. (2025120)
- Roles
- Manufacturer
- First device listed
- June 12, 2009
- Registered through
- 2026
- Brand names listed
- PerioLase MVP-7
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 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 |
|---|---|---|---|---|---|---|
| July 12, 2019 | K182930 | PerioLase Nd:YAG Pulsed Dental Laser System | GEX | Substantially Equivalent | Millennium Dental Technologies, Inc. | accessdata.fda.gov |
| March 15, 2016 | K151763 | PerioLase Nd:YAG Pulsed Dental Laser System | GEX | Substantially Equivalent | Millennium Dental Technologies, Inc. | accessdata.fda.gov |
| July 26, 2004 | K030290 | PERIOLASE ND:YAG DENTAL LASER SYSTEM | GEX | Substantially Equivalent | Millennium Dental Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 12, 2019. 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.