FDA device listing

patient examination glove,Vinyl

FDA device listing 1201733867 · opus gloves co.,ltd.

Key facts

Proprietary names patient examination glove,Vinyl
Owner/operator opus gloves co.,ltd.
Owner/operator number 10057196
Product codes LYZ
Device names LYZ - Vinyl Patient Examination Glove
Device class Class I
Classification regulations (21 CFR) 880.6250
Review panels General Hospital
Registered establishments OPUS GLOVES CO.,LTD.
Establishment registrations 3014345238
FEI numbers 3014345238
Establishment operations Contract 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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