FDA device listing

Canary Medical Gait Parameters

FDA device listing 1521121816 · Canary Medical, Inc.

Key facts

Proprietary names Canary Medical Gait Parameters
Owner/operator Canary Medical, Inc.
Owner/operator number 10082445
Product codes KQW
Device names KQW - Goniometer, Nonpowered
Device class Class I
Classification regulations (21 CFR) 888.1520
Review panels Orthopedic
Registered establishments CANARY MEDICAL USA LLC
Establishment registrations 3015802419
FEI numbers 3015802419
Establishment operations Complaint File Establishment, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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