NEUROS MEDICAL INC.

FDA Device Registration & Listing · Arden Hills, MN, US · Registration 3026283936

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
3026283936
FEI Number
3026283936
Entity Name
NEUROS MEDICAL INC.
City/State/Country
Arden Hills, MN, US
Establishment Address
1212 Red Fox Rd, Arden Hills, MN 55112, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Neuros Medical Inc. (Owner Number: 10091346)
Owner / Operator Contact Address
26800 Aliso Viejo Pkwy. Suite 250, Aliso Viejo, CA 92656, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P230020

All Registered Proprietary Names

Altius IPG Altius Cuff Small Altius Cuff Large Altius BC Altius PTC Altius IPG Accessory Kit Altius PAPC Altius PW Altius Cuff Medium

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
SAZ Stimulator, Nerve Terminus, Totally Implanted For Chronic Intractable Post-Amputation Pain Of The Lower Limb Unknown Class 3 N/A 2024-08-31

Official Correspondent

Melanie Parravi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Neuros Medical Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026283936. Last updated year: 2026. Please use registration number 3026283936 when referencing this establishment in official correspondence.
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