Data / Medical devices / United States / Fusmobile, Inc
Fusmobile, Inc: FDA-registered device maker in Alpharetta, GA, United States, 1 510(k) clearance
Fusmobile, Inc is registered with the FDA (registration 3019585303) in Alpharetta, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 14, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3019585303
- Address
- 6120 Windward Pkwy Ste 210, Alpharetta, GA, United States, 30005
- Owner or operator
- FUSMobile, INC (10094310)
- Roles
- Manufacturer
- First device listed
- November 23, 2025
- Registered through
- 2026
- Brand names listed
- Neurolyser XR
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| High Intensity Focused Ultrasound System For Peripheral Neural Tissue Ablation | SGN | 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 |
|---|---|---|---|---|---|---|
| November 14, 2025 | DEN250015 | Neurolyser XR (NXR100) | SGN | Unknown | Fusmobile, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 14, 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.