Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003000761

FEI Number

3003000761

Entity Name

TORNADO PLASTICS

City/State/Country

St-Laurent Quebec, CA

Establishment Address

4805 rue Bourg, St-Laurent Quebec H4T1H9, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Tornado Plastics (Owner Number: 10037365)

Owner / Operator Contact Address

4805 rue Bourg, St-Laurent, CA-QC H4T1H9, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DIGITAL SENSOR SHEATH PHOSPHOR PLATE PROTECTOR FLEX-BITE TAB INTRA ORAL CAMERA SHEATHS Face Shield Tornado Plastics TIPP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EGZ	Holder, Film, X-Ray	Dental	Class 1	872.1905	2011-07-07
KPY	Shield, Protective, Personnel	Radiology	Class 1	892.6500	2020-07-23

Official Correspondent

Gerald Gestetner

US Agent Details

Joseph Gestetner Business: Tornado Plastics Inc Email: jgestetner@integritynrg.com Phone: (732) 2320159

Related Public Records

Same Entity

Tornado Plastics

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003000761. Last updated year: 2026. Please use registration number 3003000761 when referencing this establishment in official correspondence.