GEBRUDER RENGGLI, AG

FDA Device Registration & Listing · Schaffhausen, CH · Registration 3009538961

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
3009538961
FEI Number
3009538961
Entity Name
GEBRUDER RENGGLI, AG
City/State/Country
Schaffhausen, CH
Establishment Address
Schweizerbildstrasse 57, CH-8200, Schaffhausen 8200, CH
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Gebruder Renggli AG (Owner Number: 10039756)
Owner / Operator Contact Address
Schweizerbildstrasse 57, CH-8200, Schaffhausen, CH-SH 8200, CH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Schlauchset, Absaugung, DS Schlauchset, Absaugung, BS OptraSculpt C-MAS S Videolaryngoskop MAC #3 C-MAS Videolaryngoskop MAC #4 C-MAS Videolaryngoskop D-BLADE Cavifil Injector

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAZ Tubing, Noninvasive General Hospital Class 2 880.6740 2020-04-15
KXR Applicator, Resin Dental Class 1 872.3140 2012-02-08
CCW Laryngoscope, Rigid Anesthesiology Class 1 868.5540 2018-11-28
DZN Instruments, Dental Hand Dental Class 1 872.4565 2012-02-08

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Gebruder Renggli AG
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
K910471 Baxter Healthcare Corp MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE 1991-03-08

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0144-2024 Covidien 1
Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024 Covidien 1
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009538961. Last updated year: 2026. Please use registration number 3009538961 when referencing this establishment in official correspondence.
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