Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002404380

FEI Number

3002404380

Entity Name

FERNO CANADA, INC.

City/State/Country

Oakville Ontario, CA

Establishment Address

2715 Bristol Circle, #2, Oakville Ontario L6H 6X5, CA

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device,Repack or Relabel Medical Device

Owner / Operator

Ferno Canada, Inc. (Owner Number: 10038140)

Owner / Operator Contact Address

2715 Bristol Circle #2, Oakville, CA-ON L6H6X5, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

132 Manta Rescue Aid Model 44 Rescue Seat 44c Rescue Seat Ferno Frac Splint Ferno Frac Care Kit Model 678 Pedimate 679 Neomate restraint LBS Restraint 773 Restraint series 471 Flotation Collar 675 Neomate Restraint 417-1 Restraint series 430 Restraint series ECMO Restraint 678 Pedimate Plus Restraint 678 Pedimate Infant Restraint 414 Restraint series 430P Restraint series 436 Swivel Speed Clip Restraint series 44 Rescue Seat series

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPP	Stretcher, Hand-Carried	General Hospital	Class 1	880.6900	2012-03-06
NOC	Splint, Extremity, Non-Inflatable, External, Non-Sterile	General, Plastic Surgery	Class 1	878.3910	2013-09-24
NZD	Stretcher, Patient Restraint	General Hospital	Class 1	880.6900	2011-09-19

Official Correspondent

Dorothy Ramsey

US Agent Details

Dorothy Ramsey Business: Ferno-Washington, Inc. Email: d.ramsey@ferno.com Phone: (937) 2832885

Related Public Records

Same Entity

Ferno Canada, Inc.

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 3002404380. Last updated year: 2026. Please use registration number 3002404380 when referencing this establishment in official correspondence.