FDA device listing

YIGAO

FDA device listing 1298276635 · TAICANG YIGAO MEDICAL TECHNOLOGY CO.,LTD

Key facts

Proprietary names YIGAO
Owner/operator TAICANG YIGAO MEDICAL TECHNOLOGY CO.,LTD
Owner/operator number 10091518
Product codes KDD
Device names KDD - Kit, Surgical Instrument, Disposable
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments TAICANG YIGAO MEDICAL TECHNOLOGY CO.,LTD
Establishment registrations 3033796310
FEI numbers 3033796310
Establishment operations 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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