FDA device listing

Arthrex Plates, Screws, and Staples

FDA device listing 1860300877 · ARTHREX, INC.

Key facts

Proprietary names Arthrex Plates, Screws, and Staples
Owner/operator ARTHREX, INC.
Owner/operator number 1220287
Premarket submissions K150456
Product codes HRS, HWC, JDR
Device names HRS - Plate, Fixation, Bone, HWC - Screw, Fixation, Bone, JDR - Staple, Fixation, Bone
Device class Class II
Classification regulations (21 CFR) 888.3030, 888.3040
Review panels Orthopedic
Registered establishments Arthrex Australia Pty Ltd., Arthrex Chile SPA, Arthrex Distribution Hub EMEA B.V., Arthrex do Brazil Importacao e Comercio de Equipamentos Medicos Ltda, Arthrex GmbH, Arthrex, Inc., ARTHREX, INC., Arthrex Korea Ltd., Arthrex Manufacturing Inc., Arthrex Mexico, S.A. de C.V., Arthrex New Zealand Limited, Arthrex (Shanghai) Co., Ltd. and 1 more
Establishment registrations 1220246, 3002579136, 3010331645, 3011230048, 3013700547, 3014004349, 3014262693, 3015231789, 3015974593, 3016851379, 3019269298, 3020704423, 3027339877
FEI numbers 1220246, 3002579136, 3010331645, 3011230048, 3013700547, 3014004349, 3014262693, 3015231789, 3015974593, 3016851379, 3019269298, 3020704423, 3027339877
Establishment operations Contract Manufacturer, Contract Sterilizer, Foreign Exporter, Specification Developer
Registration valid through 2026

At a glance

  • 10–99 Registered establishments listing this device
  • None UDI devices (GUDID) under the same submission
  • 10–99 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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