OPED GmbH

FDA Device Registration & Listing · Valley/Oberlaindern Bavaria, DE · Registration 3009718162

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
3009718162
FEI Number
3009718162
Entity Name
OPED GmbH
City/State/Country
Valley/Oberlaindern Bavaria, DE
Establishment Address
Medizinpark 1, Valley/Oberlaindern Bavaria 83626, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
OPED GmbH (Owner Number: 10041313)
Owner / Operator Contact Address
Medizinpark 1, Valley/Oberlaindern, DE-BY 83626, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Orthelligent Vision Orthelligent Pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQI Orthosis, Limb Brace Physical Medicine Class 1 890.3475 2012-07-11
KQX Goniometer, Ac-Powered Orthopedic Class 1 888.1500 2020-02-07
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2026-02-19

Official Correspondent

No official correspondent registered.

US Agent Details

Tina Caslin Business: OPED Medical, Inc. Email: t.caslin@opedmedical.com Phone: (800) 3341906

Related Public Records

Same Entity

OPED 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 3009718162. Last updated year: 2026. Please use registration number 3009718162 when referencing this establishment in official correspondence.
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