FDA device listing

Electrode Wire and Cable

FDA device listing 1046316255 · HOME CARE TECHNOLOGY CO., LTD.

Key facts

Proprietary names Electrode Wire and Cable
Owner/operator HOME CARE TECHNOLOGY CO., LTD.
Owner/operator number 9044639
Product codes IKD
Device names IKD - Cable, Electrode
Device class Class II
Classification regulations (21 CFR) 890.1175
Review panels Physical Medicine
Registered establishments HOME CARE TECHNOLOGY CO., LTD.
Establishment registrations 9710580
FEI numbers 3003514353
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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