Data / Medical devices / United States / CPMT Laser Usa LLC
CPMT Laser Usa LLC: FDA-registered device maker in Miami, FL, United States, 7 510(k) clearances
CPMT Laser Usa LLC is registered with the FDA (registration 3044175602) in Miami, FL, United States. It lists 3 device types. The FDA files 7 510(k) clearances under its listings, the newest dated February 25, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3044175602
- Address
- 2828 Coral Way Ste 312, Miami, FL, United States, 33145
- Owner or operator
- CPMT Laser USA LLC (10095667)
- Roles
- Manufacturer
- First device listed
- April 14, 2026
- Registered through
- 2026
- Brand names listed
- Ares, Armo, CANLASE, CPMT AquaPro, CPMT Ares, CPMT Facial, CPMT Grace Plus, CPMT NYX Plus and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Brush, Dermabrasion, Powered | GFE | 1 | Manufacturer | accessdata.fda.gov |
| Powered Laser Surgical Instrument | GEX | 2 | Manufacturer | accessdata.fda.gov |
| Stimulator, Muscle, Powered, For Muscle Conditioning | NGX | 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 |
|---|---|---|---|---|---|---|
| February 25, 2025 | K241601 | EMS (FlexPulse, MagnaCore, Magnetika) | NGX | Substantially Equivalent | Cpmt Laser (Canadian Pioneer Medical Technology Corporation) | accessdata.fda.gov |
| April 16, 2024 | K232133 | Co2 Laser System, Models: PureLase And VanLase | GEX | Substantially Equivalent | Cpmt Laser (Canadian Pioneer Medical Technology Corporation) | accessdata.fda.gov |
| November 17, 2022 | K222673 | Alexandrite and Nd:YAG Laser models CANLASE and TORLASE | GEX | Substantially Equivalent | Canadian Pioneer Medical Technology Corporation (Cpmt Laser) | accessdata.fda.gov |
| November 15, 2022 | K222915 | Quadruple Laser System , Models : CPMT ARES , CPMT NEMESIS , CPMT NYX PLUS , CPMT GRACE PLUS | GEX | Substantially Equivalent | Canadian Pioneer Medical Technology Corporation (Cpmt Laser) | accessdata.fda.gov |
| February 25, 2022 | K211722 | Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares | GEX | Substantially Equivalent | Canadian Pioneer Medical Technology Corporation | accessdata.fda.gov |
| October 25, 2021 | K212793 | Laser Treatment System, Model: Hera, Armo | GEX | Substantially Equivalent | Canadian Pioneer Medical Technology Corporation | accessdata.fda.gov |
| February 26, 2021 | K210033 | Laser Treatment System, Model: NYX and Grace | GEX | Substantially Equivalent | Canadian Pioneer Medical Technology Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Brush, Dermabrasion, Powered
- All makers of Stimulator, Muscle, Powered, For Muscle Conditioning
Updated February 25, 2025. 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.