Market Intelligence

Canada

Medical device market intelligence for Canada. Regulatory changes, competitor moves, and procurement trends.

180
Signals / 7 days
405
Activity Score
Health Canada
MDEL · Medical Device Licence

Recent signals

com_launch2026-05-28

Philips partners with Disney to enhance pediatric MRI experiences globally, reducing anxiety and improving workflow.

HIT Consultant · 2026-05-28
com_launch2026-05-28

Study compares Blanketrol III and Arctic Sun for cooling non-shivering patients during myocardial infarctions.

ClinicalTrials.gov · 2020-03-01
com_launch2026-05-27

A terminated study evaluated a new suction device for upper gastrointestinal bleeding during endoscopy.

ClinicalTrials.gov · 2015-04-01
reg_registration2026-05-25

NUMED CANADA, INC. has registered a medical device with the FDA under product code DQY.

FDA Device Registration & Listing ·
reg_registration2026-05-25

FDA registered 2745-3083 QUEBEC, INC. under product code LPL for two products.

FDA Device Registration & Listing ·
mkt_report2026-05-22

A pilot study is recruiting participants to assess digital tools for monitoring treatment-resistant depression.

ClinicalTrials.gov · 2024-12-16
saf_notice2026-05-21

Cincinnati Surgical sold unlicensed class II medical devices in Canada, lacking the required MDL.

Health Canada · 2026-05-21
com_ma2026-05-20

M&A and divestitures are reshaping MedTech strategies, emphasizing market access for sustained growth and valuation.

MedTech Intelligence · 2026-05-20
reg_enforcement2026-05-20

A study compared ACL graft tension using a commercial device versus physician-applied tension during surgery.

ClinicalTrials.gov · 2010-12-01
reg_registration2026-05-19

ONVET MEDICAL CANADA INC is registered with the FDA under product code EHK.

FDA Device Registration & Listing ·
reg_registration2026-05-19

7051395 Canada Inc Dba HTA Direct Sourcing has registered with the FDA under product code JIT.

FDA Device Registration & Listing ·
reg_registration2026-05-19

Ottobock SE & Co. KGaA registered a medical device with the FDA under product code KGH.

FDA Device Registration & Listing ·
reg_registration2026-05-19

Diagnostics Biochem Canada, Inc. has FDA registration 8010132 for product code CGI.

FDA Device Registration & Listing ·
mkt_report2026-05-18

A clinical trial is recruiting to assess enhanced vital sign monitoring for post-surgery patients' outcomes.

ClinicalTrials.gov · 2025-11-17
com_launch2026-05-15

A study completed on the REOM device for measuring lung mechanics in COPD patients shows agreement with traditional methods.

ClinicalTrials.gov · 2023-08-01
com_launch2026-05-15

A study validated a continuous respiratory rate measurement device to improve monitoring in hospitalized patients.

ClinicalTrials.gov · 2021-11-17
sup_procurement2026-05-14

GHX awarded health systems and leaders for excellence in supply chain performance on May 13.

Beckers Hospital Review · 2026-05-14
com_launch2026-05-14

The RPM™ system enables continuous remote monitoring of vital signs, improving patient care and reducing costs.

ClinicalTrials.gov · 2007-10-01
com_launch2026-05-13

A new device for moving patients with respiratory failure is under study for ICU use and economic analysis.

ClinicalTrials.gov · 2021-05-15
com_launch2026-05-13

The UMOX device offers an alternative to face masks for preoxygenation, showing variable effectiveness in a study.

ClinicalTrials.gov · 2009-09-01

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