FDA device listing

Aspen,Bard-Parker,instrument tray,Tray, Surgical, Instrument,Wire Nest

FDA device listing 1091439111 · Medtronic, Inc.

Key facts

Proprietary names Aspen,Bard-Parker,instrument tray,Tray, Surgical, Instrument,Wire Nest
Owner/operator Medtronic, Inc.
Owner/operator number 2112641
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 MEDICREA INTERNATIONAL, Medtronic (Changzhou) Medical Devices Technology Co., Ltd, Medtronic Engineering and Innovation Center (MEIC), MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH, MEDTRONIC SOFAMOR DANEK USA, INC., MEDTRONIC XOMED, INC., WARSAW ORTHOPEDIC, INC.
Establishment registrations 1030489, 1045254, 1824199, 1000432246, 3003120897, 3005677016, 3011795235, 3018094310
FEI numbers 1045254, 1824199, 1000432246, 1000477302, 3003120897, 3005677016, 3011795235, 3018094310
Establishment operations Complaint File Establishment, Manufacturer, Repackager/Relabeler, 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

Browse all FDA device listings