BENTEC Endoscopy GmbH

FDA Device Registration & Listing · Rietheim-Weilheim Baden-Wurttemberg, DE · Registration 1000343527

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
1000343527
FEI Number
1000343527
Entity Name
BENTEC Endoscopy GmbH
City/State/Country
Rietheim-Weilheim Baden-Wurttemberg, DE
Establishment Address
Hinteres Oeschle 6, Rietheim-Weilheim Baden-Wurttemberg 78604, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
BENTEC Endoscopy GmbH (Owner Number: 10053828)
Owner / Operator Contact Address
Hinteres Oeschle 6, Rietheim-Weilheim, DE-BW 78604, 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
OCZ Endoscopic Grasping/Cutting Instrument, Non-Powered Gastroenterology, Urology Class 2 876.1500 2025-04-18
FGA Kit, Nephroscope Gastroenterology, Urology Class 2 876.1500 2025-04-18
GCP Endoscope, Ac-Powered And Accessories Gastroenterology, Urology Class 2 876.1500 2017-01-16

Official Correspondent

Desiree Bacher

US Agent Details

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

Related Public Records

Same Entity

BENTEC Endoscopy 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
K923489 Cox Medical Ent., Inc. COX DISPOSABLE RETRIEVAL DEVICES 1992-09-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0015-2023 Hobbs Medical, Inc. 2
Hobbs Medical Polypectomy Snare Catalog Number: 4563
Z-0016-2023 Hobbs Medical, Inc. 2
Hobbs Medical Polypectomy Snare Catalog Number: 4564
Z-0026-2023 Hobbs Medical, Inc. 2
Hobbs Helical Retrieval Basket Catalog Number: 4806
Z-0027-2023 Hobbs Medical, Inc. 2
Hobbs Helical Retrieval Basket Catalog Number: 4808
Z-0028-2023 Hobbs Medical, Inc. 2
Hobbs Helical Retrieval Basket Catalog Number: 4814

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3006546082 KARL STORZ SE & CO. KG TUTTLINGEN Baden-Wurttemberg, DE
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000343527. Last updated year: 2026. Please use registration number 1000343527 when referencing this establishment in official correspondence.
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