FDA device listing

Lumbar Orthosis

FDA device listing 1805871848 · Fung Lead Medical & Sports Co., Ltd.

Key facts

Proprietary names Lumbar Orthosis
Owner/operator Fung Lead Medical & Sports Co., Ltd.
Owner/operator number 10044100
Product codes IQE
Device names IQE - Orthosis, Lumbar
Device class Class I
Classification regulations (21 CFR) 890.3490
Review panels Physical Medicine
Registered establishments FUNG LEAD MEDICAL & SPORTS CO., LTD.
Establishment registrations 3009009512
FEI numbers 3009009512
Establishment operations Foreign Exporter, Manufacturer
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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