FDA device listing

Mechanical Wheelchair

FDA device listing 1023575201 · Kunshan Hi-Fortune Health Products Co., Ltd.

Key facts

Proprietary names Mechanical Wheelchair
Owner/operator Kunshan Hi-Fortune Health Products Co., Ltd.
Owner/operator number 10036888
Premarket submissions K163352
Product codes IOR
Device names IOR - Wheelchair, Mechanical
Device class Class I
Classification regulations (21 CFR) 890.3850
Review panels Physical Medicine
Registered establishments Kunshan Hi-Fortune Health Products Co., Ltd.
Establishment registrations 3009265647
FEI numbers 3009265647
Establishment operations Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes 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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