Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022747125

FEI Number

3022747125

Entity Name

Stehle Medizintechnik

City/State/Country

Renquishausen Baden-Wurttemberg, DE

Establishment Address

Steigstr. 7, Renquishausen Baden-Wurttemberg 78603, DE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

MEDICON, E.G. (Owner Number: 10094641)

Owner / Operator Contact Address

Gaensaecker 15, Tuttlingen, DE-BW 78532, DE

Initial Importer Flag

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
GDJ	Clamp, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2025-12-12
KAE	Forceps, Ent	Ear, Nose, Throat	Class 1	874.4420	2025-12-12
HRQ	Hemostat	General, Plastic Surgery	Class 1	878.4800	2025-12-12
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2025-12-12

Official Correspondent

Mario Waizenegger

US Agent Details

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

Related Public Records

Same Entity

MEDICON, E.G.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3002862271	Wenzler Medizintechnik GmbH	Frittlingen Baden-Wurttemberg, DE
3013497507	Teufel & Gerlach GmbH	Tuttlingen Baden-Wurttemberg, DE
3003322138	Kreidler Medizintechnik GmbH	Wurmlingen Baden-Wurttemberg, DE
8010099	MEDICON, E.G.	TUTTLINGEN Baden-Wurttemberg, DE

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

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2014	Aesculap, Inc.	1	UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.

Similar Registrations

Registration Number	Establishment Name	Location
2027754	OSTEOMED	ADDISON, TX, US
9611283	DIMEDA INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE
2084346	MARINA MEDICAL INSTRUMENTS, INC.	Davie, FL, US
3004892425	SPARTECH INSTRUMENTS & CO.	SIALKOT, PUNJAB, PK
3004111573	Sterigenics US LLC	Grand Prairie, TX, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022747125. Last updated year: 2026. Please use registration number 3022747125 when referencing this establishment in official correspondence.