Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016610659

FEI Number

3016610659

Entity Name

HALOSENSE INC

City/State/Country

London Ontario, CA

Establishment Address

48 Knights Bridge Rd, London Ontario N6K 3R4, CA

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Halosense Inc (Owner Number: 10075228)

Owner / Operator Contact Address

48 Knights Bridge Rd, London, CA-ON N6K 3R4, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SaltAir

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KFZ	Humidifier, Non-Direct Patient Interface (Home-Use)	Anesthesiology	Class 1	868.5460	2020-06-09

Official Correspondent

No official correspondent registered.

US Agent Details

Wen Wang Business: Willow Glen Consultancy LLC Email: Wen.Wang@WillowGlenFDA.com Phone: (619) 8690249

Related Public Records

Same Entity

Halosense 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 3016610659. Last updated year: 2026. Please use registration number 3016610659 when referencing this establishment in official correspondence.