510(k) Report

FDA applicant

Canary Medical, Inc.

Vancouver, CA1 decision2021–20210 recalls

FDA records 1 decision for Canary Medical, Inc. (Vancouver, CA) in 2021: 1 De Novo grant. All are in product code QPP (Implantable Post-Surgical Kinematic…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Canary Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Canary Medical, Inc. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Canary Medical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Which product codes does it file in?

  • QPPImplantable Post-Surgical Kinematic Measurement Knee Device1decision

Who builds on its devices?

Later devices cite its devices 3 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • DEN200064Canary Tibial Extension with Canary Health Implanted Reporting Processor (CHIRP) SystemCanary Medical, Inc. · 20213cite it

What has FDA decided for it lately?

  • DEN200064Canary Tibial Extension with Canary Health Implanted Reporting Processor (CHIRP) SystemCanary Medical, Inc. · 2021

The one decision as Canary Medical, Inc. →

Other applicant names beginning “Canary”

FDA records each applicant name separately; these may or may not be the same firm.

Canary Medical USA, LLC 3