UNIPROX GMBH & CO. KG

FDA Device Registration & Listing · Zeulenroda-Triebes Thuringia, DE · Registration 3008564931

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
3008564931
FEI Number
3008564931
Entity Name
UNIPROX GMBH & CO. KG
City/State/Country
Zeulenroda-Triebes Thuringia, DE
Establishment Address
Heinrich-Heine-Str. 4, Zeulenroda-Triebes Thuringia 07937, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Uniprox GmbH & Co. KG (Owner Number: 10033647)
Owner / Operator Contact Address
Heinrich-Heine-Str. 4, Zeulenroda-Triebes, DE-TH 07937, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Uniprox F90 Multiaxial carbon fibre foot Uniprox F310 Chopart Uniprox F360 High-Profile Uniprox F340 Mid-Profile

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISH Component, External, Limb, Ankle/Foot Physical Medicine Class 1 890.3420 2010-09-10

Official Correspondent

No official correspondent registered.

US Agent Details

Michael Cannon Business: Bauerfeind USA, Inc. Email: mcannon@bauerfeindusa.com Phone: (703) 5877825

Related Public Records

Same Entity

Uniprox GmbH & Co. KG
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 3008564931. Last updated year: 2026. Please use registration number 3008564931 when referencing this establishment in official correspondence.
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