FDA device listing

TRAY, SURGICAL, INSTRUMENT

FDA device listing 1405829422 · Aegis Spine

Key facts

Proprietary names TRAY, SURGICAL, INSTRUMENT
Owner/operator Aegis Spine
Owner/operator number 10031416
Product codes FSM
Device names FSM - Tray, Surgical, Instrument
Device class Class I
Classification regulations (21 CFR) 878.4800
Review panels General & Plastic Surgery
Registered establishments AEGIS MEDITEC, INC.
Establishment registrations 3009790163
FEI numbers 3009790163
Establishment operations Specification Developer
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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