FUSMOBILE, INC

FDA Device Registration & Listing · Alpharetta, GA, US · Registration 3019585303

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3019585303
FEI Number
3019585303
Entity Name
FUSMOBILE, INC
City/State/Country
Alpharetta, GA, US
Establishment Address
6120 Windward Pkwy Ste 210, Alpharetta, GA 30005, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FUSMobile, INC (Owner Number: 10094310)
Owner / Operator Contact Address
6120 Windward Parkway, Suite 210, Alpharetta, GA 30005, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
DEN250015
PMA Number
N/A

All Registered Proprietary Names

Neurolyser XR

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SGN High Intensity Focused Ultrasound System For Peripheral Neural Tissue Ablation Neurology Class 2 882.4420 2025-11-23

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FUSMobile, INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019585303. Last updated year: 2026. Please use registration number 3019585303 when referencing this establishment in official correspondence.
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