Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006655502

FEI Number

3006655502

Entity Name

WEGAMED GMBH

City/State/Country

Essen North Rhine-Westphalia, DE

Establishment Address

Am Zehnthof 189, Essen North Rhine-Westphalia D-45307, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Wegamed GmbH (Owner Number: 10024339)

Owner / Operator Contact Address

Am Zehnthof 189, Essen, DE-NOTA D-45307, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Med Matrix Med Select Check Medical Sport Test Expert Plus

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HCC	Device, Biofeedback	Neurology	Class 2	882.5050	2008-01-22

Official Correspondent

Peter Molleney

US Agent Details

Lavanya Rastogi Business: Wegamed USA Email: leo.rastogi@outlook.com Phone: (919) 5239767

Related Public Records

Same Entity

Wegamed GmbH

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
K873418	Bodylog, Inc.	BODYLOG STRESS REDUCTION PACKAGE	1987-12-17
K792659	Bio-Feedback Systems, Inc.	FEEDBACK EDR SYSTEM MODEL ME-1	1980-01-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006655502. Last updated year: 2026. Please use registration number 3006655502 when referencing this establishment in official correspondence.