GENERAL MEDICAL CO.

FDA Device Registration & Listing · Jacksonville, FL, US · Registration 3013399500

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
3013399500
FEI Number
3013399500
Entity Name
GENERAL MEDICAL CO.
City/State/Country
Jacksonville, FL, US
Establishment Address
5011 Gate Parkway, Bldg. 100, Suite 100, Jacksonville, FL 32256, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
GENERAL MEDICAL CO. (Owner Number: 2012353)
Owner / Operator Contact Address
5011 Gate Parkway, Bldg. 100, Suite 100, Jacksonville, FL 32256, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EGJ Device, Iontophoresis, Other Uses Physical Medicine Class 2 890.5525 2015-12-14

Official Correspondent

Emma Stewart

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GENERAL MEDICAL CO.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K842483 Santa Barbara Medco, Inc. SANTA BARBARA MEDCO-LANTOPHORETIC APPLIC 1984-08-31

Similar Registrations

Registration Number Establishment Name Location
3015099059 DERMADRY LABORATORIES INC. Montreal Quebec, CA
2183164 Cardinal Health Wabasha, MN, US
3017264244 DJO, LLC Carlsbad, CA, US
2025066 AXELGAARD MFG. CO., LTD. FALLBROOK, CA, US
3009736547 Laser Marketing Group, LLC Lehi, UT, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013399500. Last updated year: 2026. Please use registration number 3013399500 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.