I.C.LERCHER-SOLUTIONS GMBH

FDA Device Registration & Listing · Stockach Baden-Wurttemberg, DE · Registration 3014273912

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
3014273912
FEI Number
3014273912
Entity Name
I.C.LERCHER-SOLUTIONS GMBH
City/State/Country
Stockach Baden-Wurttemberg, DE
Establishment Address
Im Saengenloh 8, Stockach Baden-Wurttemberg 78333, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
I.C.LERCHER-Solutions GmbH (Owner Number: 10059333)
Owner / Operator Contact Address
Im Saengenloh 8, Stockach, DE-BW 78333, 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
FWJ Camera, Cine, Microsurgical, Without Audio General, Plastic Surgery Class 1 878.4160 2018-12-21
HPP Headlamp, Operating, Battery-Operated Ophthalmic Class 1 886.4335 2018-12-21
HJN Transilluminator, Battery-Powered Ophthalmic Class 1 886.1945 2018-12-21
EQL Laryngostroboscope Ear, Nose, Throat Class 1 874.4750 2018-12-21
HJH Loupe, Binocular, Low Power Ophthalmic Class 1 886.5120 2019-01-02

Official Correspondent

Nico Gleichauf

US Agent Details

Beate Weiss-Krull Business: Beate Weiss-Krull, Attorney at Law Email: bea@weisskrull-law.com Phone: (503) 2340355

Related Public Records

Same Entity

I.C.LERCHER-Solutions 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-2412-2024 Alcon Research LLC Aspex Facility 1
Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014273912. Last updated year: 2026. Please use registration number 3014273912 when referencing this establishment in official correspondence.
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