Medical device reports and publications

Under the Food and Drugs Act, medical devices are health or medical instruments used in the treatment, mitigation, diagnosis or prevention of a disease or abnormal physical condition.

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Reports and publications

This section contains links to reports and publications related to medical devices, including:

Medical devices performance reports

The medical devices performance reports provide detailed data about the timeliness of pre-market medical devices review process against the performance service standards. Each report is organized by parts of the regulations and the types of applications they include.
The reports include statistics by submission type, showing:

Key terms explained

Applications received:
The number of submissions received during the reporting period.
Workload:
The number of submissions "in process" on a given day.
Backlog:
The proportion of the workload that exceeds target timelines. (Note: "Workload" is sometimes confused with the amount of work received, which can cause misunderstanding.)
Licences issued:
A count of applications licenced after completion of scientific review.
Decisions:
Points in the process where an action is recommended to license, reject, refuse, or request additional information, in regards to the application.
First decision:
Time from acceptance for review to either a licence being issued or a request for more additional information.
Second decisions:
Time from receiving a response to an additional information request to either issuing a license or making a subsequent additional information request.

Annual reports

2024-2025

For annual reports from 2013 to 2024, contact publications@hc-sc.gc.ca.

Quarterly reports

2025-2026

2024-2025

For quarterly reports from 2017 to 2023, contact publications@hc-sc.gc.ca.

Contact us

For more information about the reports, contact the Medical Devices Directorate.
Email: meddevices-instrumentsmed@hc-sc.gc.ca

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2025-09-12