TUNAP GMBH & CO. KG

FDA Device Registration & Listing · Wolfratshausen Bavaria, DE · Registration 3014471275

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
3014471275
FEI Number
3014471275
Entity Name
TUNAP GMBH & CO. KG
City/State/Country
Wolfratshausen Bavaria, DE
Establishment Address
Buergermeister-Seidl-Strasse 2, Wolfratshausen Bavaria 82515, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
TUNAP GmbH & Co. KG (Owner Number: 10057729)
Owner / Operator Contact Address
Buergermeister-Seidl-Strasse 2, Wolfratshausen, DE-BY 82515, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
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
EFB Handpiece, Air-Powered, Dental Dental Class 1 872.4200 2021-03-22

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: REGISTRAR CORP Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

TUNAP GmbH & Co. KG
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
K212910 Shenzhen Carejoy Technology Co., Ltd. Dental High-speed Turbine Handpiece, Dental Low-speed Turbine Handpiece 2022-11-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014471275. Last updated year: 2026. Please use registration number 3014471275 when referencing this establishment in official correspondence.
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