LK MECHANIK UND BLECHVERARBEITUNG GMBH

FDA Device Registration & Listing · Huettenberg-Rechtenbach Hesse, DE · Registration 3010461759

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
3010461759
FEI Number
3010461759
Entity Name
LK MECHANIK UND BLECHVERARBEITUNG GMBH
City/State/Country
Huettenberg-Rechtenbach Hesse, DE
Establishment Address
Budenweisgraben 9, Huettenberg-Rechtenbach Hesse 35625, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
LK MECHANIK UND BLECHVERARBEITUNG GMBH (Owner Number: 10045003)
Owner / Operator Contact Address
Budenweisgraben 9, Huettenberg-Rechtenbach, DE-HE 35625, 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
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2013-09-10

Official Correspondent

No official correspondent registered.

US Agent Details

Angelika Scherp Email: info@bsi-fda.com Phone: (201) 3318358

Related Public Records

Same Entity

LK MECHANIK UND BLECHVERARBEITUNG GMBH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2016 Zimmer, Inc. 1
Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010461759. Last updated year: 2026. Please use registration number 3010461759 when referencing this establishment in official correspondence.
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