LOLL FEINMECHANIK GMBH

FDA Device Registration & Listing · Tornesch Schleswig-Holstein, DE · Registration 3018182995

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
3018182995
FEI Number
3018182995
Entity Name
LOLL FEINMECHANIK GMBH
City/State/Country
Tornesch Schleswig-Holstein, DE
Establishment Address
Borstelweg 16, Tornesch Schleswig-Holstein 25436, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Loll Feinmechanik GmbH (Owner Number: 10081259)
Owner / Operator Contact Address
Borstelweg 16, Tornesch, DE-SH 25436, 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
HSB Rod, Fixation, Intramedullary And Accessories Orthopedic Class 2 888.3020 2021-03-30

Official Correspondent

No official correspondent registered.

US Agent Details

Angelika Scherp Business: BSI Business Support International Email: info@bsi-fda.com Phone: (212) 3318358

Related Public Records

Same Entity

Loll Feinmechanik 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
K040336 Synthes (Usa) SYNTHES (USA) LATERAL ENTRY FEMORAL NAIL SYSTEM 2004-04-12
K083648 Efratgo, Ltd. HI Tech Bio-Surgical GOTFRIED PHYSIOLOGICAL HIP (PH) NAIL 2009-05-14
K192312 Zimmer GmbH Zimmer Natural Nail System Cephalomedullary Nails 2019-10-11
K002057 Biomet Orthopedics, Inc. BROOKER TIBIA NAILS 2000-10-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018182995. Last updated year: 2026. Please use registration number 3018182995 when referencing this establishment in official correspondence.
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