FDA device listing

Surgeon'S Gloves

FDA device listing 1877877399 · BOSMA INDUSTRIES FOR THE BLIND, INC.

Key facts

Owner/operator BOSMA INDUSTRIES FOR THE BLIND, INC.
Owner/operator number 9024211
Premarket submissions K150146
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 BOSMA INDUSTRIES FOR THE BLIND, INC.
Establishment registrations 1833700
FEI numbers 1000115586
Establishment operations Repackager/Relabeler
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 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

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