Bricon Technology GmbH

FDA Device Registration & Listing · WURMLINGEN Baden-Wurttemberg, DE · Registration 3004072627

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
3004072627
FEI Number
3004072627
Entity Name
Bricon Technology GmbH
City/State/Country
WURMLINGEN Baden-Wurttemberg, DE
Establishment Address
EISENBAHNSTRASSE 100, WURMLINGEN Baden-Wurttemberg D-78573, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Bricon Technology GmbH (Owner Number: 9100825)
Owner / Operator Contact Address
EISENBAHNSTRASSE 100, --, WURMLINGEN, DE-BW 78573, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
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
MJO Prosthesis, Intervertebral Disc Unknown Class 3 N/A 2024-10-18
PEK Spinous Process Plate Orthopedic Class 2 888.3050 2025-06-24

Official Correspondent

No official correspondent registered.

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

Bricon Technology GmbH
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 3004072627. Last updated year: 2026. Please use registration number 3004072627 when referencing this establishment in official correspondence.
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