Kirchner & Wilhelm GmbH + Co.KG

FDA Device Registration & Listing · Asperg Baden-Wurttemberg, DE · Registration 8010427

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
8010427
FEI Number
6034
Entity Name
Kirchner & Wilhelm GmbH + Co.KG
City/State/Country
Asperg Baden-Wurttemberg, DE
Establishment Address
Eberhardstrasse 56, Asperg Baden-Wurttemberg 71679, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KIRCHNER and WILHELM GmbH (Owner Number: 8010427)
Owner / Operator Contact Address
EBERHARDSTRASSE 56, --, Asperg, DE-BW 71679, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

KaWe laryngoscope KaWe LED head light H-800 KaWe stethoscopes KaWe KaWe specula KaWe MedCenter® 5000 KaWe otoscope KaWe ophthalmoscope

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCW Laryngoscope, Rigid Anesthesiology Class 1 868.5540 2001-12-27
HPP Headlamp, Operating, Battery-Operated Ophthalmic Class 1 886.4335 2012-02-27
LDE Stethoscope, Manual Cardiovascular Class 1 870.1875 2001-12-27
GWZ Percussor Neurology Class 1 882.1700 2016-09-08
FXG Specula Accessories General, Plastic Surgery Class 1 878.1800 1998-02-12
HPI Aid, Vision, Optical, Ac-Powered Ophthalmic Class 1 886.5915 2012-02-27
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 1998-02-12
HLJ Ophthalmoscope, Battery-Powered Ophthalmic Class 2 886.1570 2009-03-18
FSP Loupe, Diagnostic/Surgical General, Plastic Surgery Class 1 878.4800 2018-11-02

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Schwartz Business: mdi consultants Email: alan@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

KIRCHNER and WILHELM 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
K932506 Rudolf Riester GmbH & Co. KG RI-SCOPE (S) 1993-10-08

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0144-2024 Covidien 1
Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010427. Last updated year: 2026. Please use registration number 8010427 when referencing this establishment in official correspondence.
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