GBO MEDIZINTECHNIK AG

FDA Device Registration & Listing · Rimbach Hesse, DE · Registration 3005095860

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
3005095860
FEI Number
3005095860
Entity Name
GBO MEDIZINTECHNIK AG
City/State/Country
Rimbach Hesse, DE
Establishment Address
Kleiststrasse 6, Rimbach Hesse 64668, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
gbo Medizintechnik AG (Owner Number: 10087227)
Owner / Operator Contact Address
Kleiststrasse 6, Rimbach, DE-HE 64668, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HiToP® 1touch HiToP® 4touch HiToP® 2touch TESI

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 2023-01-31
LIH Interferential Current Therapy Neurology Class 2 882.5890 2023-01-31
GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief Neurology Class 2 882.5890 2023-01-31
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2023-03-07

Official Correspondent

No official correspondent registered.

US Agent Details

Mohammadali Nezakati Business: HILLTEK LLC Email: nezakati@hilltek.co Phone: (206) 4069390

Related Public Records

Same Entity

gbo Medizintechnik AG
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 3005095860. Last updated year: 2026. Please use registration number 3005095860 when referencing this establishment in official correspondence.
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