QUINTENZ HYBRIDTECHNIK GMBH

FDA Device Registration & Listing · Neuried Bavaria, DE · Registration 3010232390

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
3010232390
FEI Number
3010232390
Entity Name
QUINTENZ HYBRIDTECHNIK GMBH
City/State/Country
Neuried Bavaria, DE
Establishment Address
Eichenstrasse 15, Neuried Bavaria 82061, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Quintenz Hybridtechnik GmbH (Owner Number: 10042959)
Owner / Operator Contact Address
Eichenstrasse 15, Neuried, DE-BY 82061, 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
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2023-05-25
GEY Motor, Surgical Instrument, Ac-Powered General, Plastic Surgery Class 1 878.4820 2013-01-15

Official Correspondent

Michael Quintenz

US Agent Details

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

Related Public Records

Same Entity

Quintenz Hybridtechnik 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
K260601 Blue Belt Technologies, Inc. REAL INTELLIGENCE™ CORI™ 2026-03-26
K905383 Micro Surgical Instruments Corp. 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY 1991-06-18
K913369 Micro Surgical Instruments Corp. MICRO-AIRE MODEL 2060 1991-11-01

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0041-2024 Blue Belt Technologies, Inc 2
Real Intelligence CORI RI.KNEE v2.0 TKA (Total Knee Arthroplasty) software version 2.0 (2.0.0.5) Product Number: ROB10299

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010232390. Last updated year: 2026. Please use registration number 3010232390 when referencing this establishment in official correspondence.
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