Data / Medical devices / United States / Aesthetic Protools, Inc.
Aesthetic Protools, Inc.: FDA-registered device maker in Scottsdale, AZ, United States, 3 510(k) clearances
Aesthetic Protools, Inc. is registered with the FDA (registration 3043846025) in Scottsdale, AZ, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 3, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3043846025
- Address
- 8969 E Talking Stick Way Ste C-5, Scottsdale, AZ, United States, 85250
- Owner or operator
- Aesthetic ProTools, Inc. (10096292)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- August 24, 2026
- Registered through
- 2026
- Brand names listed
- BUBBL, Tri-Pulse, VADER
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Powered Laser Surgical Instrument | GEX | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Repackager or relabeler, Specification developer | 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 |
|---|---|---|---|---|---|---|
| September 3, 2025 | K251457 | Diode laser therapy device (VADER) | GEX | Substantially Equivalent | Beijing Superlaser Technology Co., Ltd. | accessdata.fda.gov |
| December 1, 2023 | K232708 | Intense pulsed light therapy device | ONF | Substantially Equivalent | Hebei Zhemai Technology Co., Ltd. | accessdata.fda.gov |
| February 22, 2017 | K161926 | ND YAG Q-switch Laser Therapy Machine | GEX | Substantially Equivalent | Beijing Adss Development Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Powered Laser Surgical Instrument
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Updated September 3, 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.