SIMMANK GmbH & Co.KG

FDA Device Registration & Listing · TUTTLINGEN Baden-Wurttemberg, DE · Registration 8010395

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
8010395
FEI Number
6032
Entity Name
SIMMANK GmbH & Co.KG
City/State/Country
TUTTLINGEN Baden-Wurttemberg, DE
Establishment Address
ETTLENSEGART 15, TUTTLINGEN Baden-Wurttemberg 78532, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
Simmank GmbH & Co. KG (Owner Number: 8010395)
Owner / Operator Contact Address
Jetterstrasse 15, --, TUTTLINGEN, DE-BW 78532, 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
GEN Forceps, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2008-01-10
JYT Pick, Microsurgical Ear Ear, Nose, Throat Class 1 874.4420 2024-01-23
NNN Crimper, Wire, Ent, Non-Sterile Ear, Nose, Throat Class 1 874.3540 2024-10-17
KTG Knife, Ent Ear, Nose, Throat Class 1 874.4420 2025-04-09
JYR Nipper, Malleus Ear, Nose, Throat Class 1 874.4420 2010-02-04
JZB Scissors, Ear Ear, Nose, Throat Class 1 874.4420 2024-02-27
GZX Instrument, Microsurgical Neurology Class 1 882.4525 1986-04-30
FCL Forceps, Biopsy, Non-Electric Gastroenterology, Urology Class 1 876.1075 1999-05-07
FHB Hook, Gastro-Urology Gastroenterology, Urology Class 1 876.4730 2024-01-23
KAE Forceps, Ent Ear, Nose, Throat Class 1 874.4420 1978-04-25

Official Correspondent

Armin Spiegel

US Agent Details

Franz Menean Business: MEDAGENT Inc. Email: mail@medagent-usa.com Phone: (603) 5702039

Related Public Records

Same Entity

Simmank GmbH & Co. KG
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
K851170 The Huxley Instrument Corp. DISSECTING TWEEZER #283-72PCS. SS 410 1985-04-25
K821248 Conphar, Inc. ROCHESTER PEAN FORCEPS 1982-05-28
K914226 E.I. Dupont DE Nemours & Co., Inc. ACA(R) BETA-2-MICROGLOBULIN (B2M) TEST PACK 1991-11-19

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8010395. Last updated year: 2026. Please use registration number 8010395 when referencing this establishment in official correspondence.
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