FDA device listing

Tray, Surgical - DeRoyal

FDA device listing 1970047134 · DEROYAL INDUSTRIES, INC.

Key facts

Proprietary names Tray, Surgical - DeRoyal
Owner/operator DEROYAL INDUSTRIES, INC.
Owner/operator number 1044833
Product codes LRP
Device names LRP - Tray, Surgical
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments DeRoyal Industries, Inc., DEROYAL INDUSTRIES, INC., Guatemala Medical Manufacturing, Ortho and Surgical Products Enterprises S.A.
Establishment registrations 1043214, 1054241, 1055236, 1057404, 1060680, 2320762, 3010452421, 3045857302
FEI numbers 1043214, 1000112877, 1000112968, 1000208576, 1000208624, 3003040625, 3010452421, 3045857302
Establishment operations Complaint File Establishment, Specification Developer, Contract Manufacturer, Repackager/Relabeler, Contract Sterilizer
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

Browse all FDA device listings