FDA device listing

Surgeon'S Gloves

FDA device listing 1194201348 · WRP ASIA PACIFIC SDN. BHD.

Key facts

Owner/operator WRP ASIA PACIFIC SDN. BHD.
Owner/operator number 8041005
Premarket submissions K111807
Product codes KGO
Device names KGO - Surgeon'S Gloves
Device class Class I
Classification regulations (21 CFR) 878.4460
Review panels General & Plastic Surgery
Registered establishments WRP ASIA PACIFIC SDN. BHD.
Establishment registrations 8041005
FEI numbers 3002808507
Establishment operations Contract Manufacturer, Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None 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

Browse all FDA device listings