Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3002912391

FEI Number

3002912391

Entity Name

BRAEBON MEDICAL CORP.

City/State/Country

KANATA Ontario, CA

Establishment Address

1-100 SCHNEIDER ROAD, KANATA Ontario K2K 1Y2, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

BRAEBON MEDICAL CORP. (Owner Number: 9041773)

Owner / Operator Contact Address

1-100 SCHNEIDER ROAD, KANATA, CA-ON K2K 1Y2, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K001743

PMA Number

N/A

All Registered Proprietary Names

ULTIMA AIRFLOW SENSOR VALUELINE AIRFLOW SENSOR Adult Airflow Thermocouple Oral Thermocouple Airflow Sensor cTherm Cannula Thermistor Ultima Breath Sensor Interface Ultima Airflow Sensor for Alice Disposable cTherm VALUELINE RESPIRATORY EFFORT SENSOR ULTIMA RESPIRATORY EFFORT SENSORS Ultima PVDF Respiratory Effort Sensor Ultima High-Output PVDF Respiratory Effort Sensor SnoreByte VALUELINE PRESSURE TRANSDUCER ULTIMA AIRFLOW PRESSURE TRANSDUCER Ultima Pressure Sensor Kit for Alice Ultima Pressure Sensor Kit Ultima Titration Sensor Kit Ultima Esophageal Differential Pressure Transducer Ultima Dual Pressure Sensor Kit PT Lite Low Gain Pressure Transducer Starter Kit PT1 Low Gain/High Gain Pressure Transducer Starter Kit PT2 Dual Differential Airflow Pressure Transducer MEDIBYTE MediByte Jr. MediOX ValueFlow Nasal Cannula + Filter OroNasal Cannula Ultima Micro Nasal Cannula ValueFlow Oral + Nasal Cannula + Filter PureFlow Duo Cannula Ultima Oral + Nasal Cannula + Filter Ultima Oral + Nasal Cannula Pneumo Flow Sensor Dual Pressure Sensor Safety Filter + Adapter Ultima Pressure Sensor Hydrophobic Filter PureFlow OroNasal Cannula PureFlow OroNasal Cannula + Filter Ultima Nasal Cannula + Filter Ultima Divided Nasal Cannula OrthoFresh CPAPFresh Q-RIP SYSTEM ULTIMA SMARTBELT KIT Disposable RIP Belt Q-RIP Belt Q-RIP Belt for Alice

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PLC	Sleep Appliances With Patient Monitoring	Dental	Class 2	872.5570	2019-05-23
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2019-05-23
BZQ	Monitor, Breathing Frequency	Anesthesiology	Class 2	868.2375	2007-11-20
BZQ	Monitor, Breathing Frequency	Anesthesiology	Class 2	868.2375	2007-11-20
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2023-06-07
BZQ	Monitor, Breathing Frequency	Anesthesiology	Class 2	868.2375	2007-11-20
MNR	Ventilatory Effort Recorder	Anesthesiology	Class 2	868.2375	2003-10-17
CAT	Cannula, Nasal, Oxygen	Anesthesiology	Class 1	868.5340	2002-06-20
JER	Cleaner, Denture, Mechanical	Dental	Class 1	872.3530	2023-08-01
BZQ	Monitor, Breathing Frequency	Anesthesiology	Class 2	868.2375	2007-11-20

Official Correspondent

No official correspondent registered.

US Agent Details

Taimi Liepert Email: Ttliepert@gmail.com Phone: (574) 2290916

Related Public Records

Same Entity

BRAEBON MEDICAL CORP.

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
K122391	Medtronic Xomed, Inc.	MEDTRONIC XOMED, INC.	2013-01-10
K913749	Edentec Corp.	EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170	1992-07-02
K771407	Research Development Corp.	LUNG VOLUME & PRESSURE MONITOR	1977-08-04
K122223	Philips Medizin Systeme Boeblingen GmbH	NEW: INTELLIVUE CL RESPIRATION POD NEW: SPECIALIZED ASSESSORY: MOBILE CL RESP ATTACHMENT MODIFIED: INTELLIVUE PATIENT MO	2013-04-12
K082968	Apneicare, LLC	APNEICARE CONNECTION CENTER/INTERNET ANALYSIS	2009-01-02

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2022	NOX MEDICAL Keldnaholt Reykjavik Iceland	2	Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep.

Similar Registrations

Registration Number	Establishment Name	Location
3009440973	SomnoMed Phillipines Inc.	Makati City National Capital Region, PH
3005598536	SOMNOMED INC.	Plano, TX, US
3013116677	PROSOMNUS SLEEP TECHNOLOGIES	Pleasanton, CA, US
3005343849	SOMNOMED, LTD.	CROWS NEST New South Wales, AU
3008186372	GCDL, LLC	Prospect Heights, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002912391. Last updated year: 2026. Please use registration number 3002912391 when referencing this establishment in official correspondence.