HomeBraceGermany GmbH

FDA Device Registration & Listing · Urbach Baden-Wurttemberg, DE · Registration 3038289351

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
3038289351
FEI Number
3038289351
Entity Name
HomeBraceGermany GmbH
City/State/Country
Urbach Baden-Wurttemberg, DE
Establishment Address
Birkenweg 12, Urbach Baden-Wurttemberg 73660, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
HomeBraceGermany GmbH (Owner Number: 10093330)
Owner / Operator Contact Address
Birkenweg 12, Urbach, DE-BW 73660, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

MyEcc Pupil Prop MyEcc MyEcc V5

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNN Components, Wheelchair Physical Medicine Class 1 890.3920 2025-04-30

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Schwartz Business: mdi Consultants, Inc. Email: alan@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

HomeBraceGermany 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 3038289351. Last updated year: 2026. Please use registration number 3038289351 when referencing this establishment in official correspondence.
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