VINZENZ SATTLER chirurgische Instrumente GMBH

FDA Device Registration & Listing · FRIDINGEN Baden-Wurttemberg, DE · Registration 8010376

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
8010376
FEI Number
3006441280
Entity Name
VINZENZ SATTLER chirurgische Instrumente GMBH
City/State/Country
FRIDINGEN Baden-Wurttemberg, DE
Establishment Address
27/1 GARTENSTRASSE, FRIDINGEN Baden-Wurttemberg 78567, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
VINZENZ SATTLER chirurgische Instrumente GMBH (Owner Number: 8010376)
Owner / Operator Contact Address
27/1 GARTENSTRASSE, --, FRIDINGEN, DE-NOTA 78567, 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
HNC Specula, Ophthalmic Ophthalmic Class 1 886.4350 2000-11-20
GAD Retractor General, Plastic Surgery Class 1 878.4800 2000-11-20
FFO Retractor, Self-Retaining Gastroenterology, Urology Class 1 876.4730 2010-03-04

Official Correspondent

LORE EPPLE

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

VINZENZ SATTLER chirurgische Instrumente 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
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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010376. Last updated year: 2026. Please use registration number 8010376 when referencing this establishment in official correspondence.
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