FDA device listing

Conmed (SX) - FENESTRATED CANNULA,Smith&Nephew3754 (NR) - 3.8mm Tapered Awl, Disposable,Smith&Nephew3754 (NR) - (5)…

FDA device listing 1438219931 · STERIS Corporation

Key facts

Proprietary names Conmed (SX) - FENESTRATED CANNULA,Smith&Nephew3754 (NR) - 3.8mm Tapered Awl, Disposable,Smith&Nephew3754 (NR) - (5) Guidewire, 1.2mmx 18” (46 cm),Smith&Nephew3754 (NR) - (6) Guidewire 2.0mm x 15,Smith&Nephew3754 (NR) - ACUFEX Clear.Trac Threadedd.10 IDx76 LTX(10),Smith&Nephew3754 (NR) BONE TUNNEL PLUG CANN 7-12MM LTX FREE (6,Smith&Nephew3754 (NR) - Clear-Trac Complete Cannula System, 4.5mm x 72mm…
Owner/operator STERIS Corporation
Owner/operator number 1527821
Product codes NBH
Device names NBH - Accessories, Arthroscopic
Device class Class I
Classification regulations (21 CFR) 888.1100
Review panels Orthopedic
Registered establishments Isomedix Operations, Inc., ISOMEDIX OPERATIONS INC, ISOMEDIX OPERATIONS INC., STERIS ISOMEDIX PUERTO RICO, INC.
Establishment registrations 1220477, 1424263, 1450662, 1526711, 1643817, 2245304, 2648623
FEI numbers 1220477, 1450662, 1526711, 1643817, 2245304, 2648623, 3003015552
Establishment operations 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

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