INTEGRATED BIOMEDICAL CORP.

FDA Device Registration & Listing · Las Vegas, NV, US · Registration 3004413879

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
3004413879
FEI Number
3004413879
Entity Name
INTEGRATED BIOMEDICAL CORP.
City/State/Country
Las Vegas, NV, US
Establishment Address
4481 W. Reno Ave, Las Vegas, NV 89118, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
INTEGRATED BIOMEDICAL CORP. (Owner Number: 9060302)
Owner / Operator Contact Address
4481 W RENO AVE, --, Las Vegas, NV 89118, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Myopulse Electro-Myopulse 75L Electro-Myopulse 55C Neuroscope Electro-Acuscope 70C Electro-Myogen Electro-Myoscope 85 Electro-Equiscope ALGONIX Electro-Acuscope 85 Electro-Acuscope 85P

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2008-03-29
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2007-12-10
IKN Electromyograph, Diagnostic Physical Medicine Class 2 890.1375 2008-03-29
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2008-03-29

Official Correspondent

DANA NEBRENSKY, M.A.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

INTEGRATED BIOMEDICAL CORP.
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
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04
K964028 Mettler Electronics Corp. SYS STIM 226 1997-02-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004413879. Last updated year: 2026. Please use registration number 3004413879 when referencing this establishment in official correspondence.
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