Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005182241

FEI Number

3005182241

Entity Name

LANDANGER

City/State/Country

CHAUMONT Haute-Marne, FR

Establishment Address

ZI La Vendue, CHAUMONT Haute-Marne 52000, FR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LANDANGER S.A. (Owner Number: 9074909)

Owner / Operator Contact Address

Z.I La Vendue, CS 52152, CHAUMONT CEDEX 9, FR-52 52906, FR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LANDANGER DELACROIX CHEVALIER LANDANGER DELACROIX-CHEVALIER Retractor TRAY, SURGICAL curette, surgical, general use

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MDM	Instrument, Manual, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2022-10-25
DWS	Instruments, Surgical, Cardiovascular	Cardiovascular	Class 1	870.4500	1995-03-27
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2021-05-03
LRP	Tray, Surgical	General, Plastic Surgery	Class 1	878.4800	2019-05-29
FZS	Curette, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2021-02-11

Official Correspondent

Alain GUILLAUMOT

US Agent Details

Michael Crawford Business: MED ALLIANCE Email: info@medallianceinternational.com Phone: (630) 4437070

Related Public Records

Same Entity

LANDANGER S.A.

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
K922626	Andronic Devices, Ltd.	ADEPT INSTRUMENT POSITIONING ACCESSORY	1992-10-19
K820290	The Anspach Effort, Inc.	SELF RETAINING RETRACTOR FOR HAND SURG	1982-03-05
K760422	Cutter Laboratories, Inc.	SURGICAL RETRACTOR	1976-08-23
K881095	CooperVision, Inc.	KOI(TM) INSTRUMENT TRAYS	1988-04-06

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0008-04	Rultract Inc	1	Rultract Surgical Retractor, 4100 Series, all system configurations, reusable.
Z-0031-2014	Aesculap, Inc.	1	UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.
Z-0036-2010	Alphatec Spine, Inc.	1	ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.
Z-0034-2012	X Spine Systems Inc	1	Axle Interspinous Fusion System Torque Driver Handle, Model #: X060-0323, Lot # 525941, S/Ns 001-017, Lot # 525942, S/Ns 001-050, Mfr. By: Bradshaw Medical Inc., Kenosha, WI 53144 The Axle Torque Driver Handle is used to lock the set screw into the locking plate.

Similar Registrations

Registration Number	Establishment Name	Location
3004358587	HURON TOOL & CUTTER GRINDING	Farmingdale, NY, US
3023809973	RUSUN MEDICAL CO., LTD	Yichun City Jiangxi, CN
3008496217	DERMATO PLASTICA BEAUTY CO., LTD.	Kaohsiung City, TW
3001614464	medi-G GMBH	Messkirch Baden-Wurttemberg, DE
3028006458	ClearPoint Neuro Inc.	Carlsbad, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005182241. Last updated year: 2026. Please use registration number 3005182241 when referencing this establishment in official correspondence.