MAX NEURO SUPPLY INC.

FDA Device Registration & Listing · Diamond Bar, CA, US · Registration 3008588921

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
3008588921
FEI Number
3008588921
Entity Name
MAX NEURO SUPPLY INC.
City/State/Country
Diamond Bar, CA, US
Establishment Address
1469 Rolling Knoll Rd, Diamond Bar, CA 91765, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Max Neuro Supply Inc. (Owner Number: 10033584)
Owner / Operator Contact Address
1469 Rolling knoll road, 1469 Rolling knoll road, Diamond Bar, CA 91765, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K072276
PMA Number
N/A

All Registered Proprietary Names

Friendship Medical

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GXZ Electrode, Needle Neurology Class 2 882.1350 2010-09-02

Official Correspondent

Edward Ma

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Max Neuro Supply 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 3008588921. Last updated year: 2026. Please use registration number 3008588921 when referencing this establishment in official correspondence.
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