FDA device listing

SHAVER SYSTEM

FDA device listing 1635148370 · ARTHREX, INC.

Key facts

Proprietary names SHAVER SYSTEM
Owner/operator ARTHREX, INC.
Owner/operator number 1220287
Premarket submissions K932699
Product codes HWE
Device names HWE - Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
Device class Class I
Classification regulations (21 CFR) 878.4820
Review panels General & Plastic Surgery
Registered establishments Arthrex Australia Pty Ltd., Arthrex California Technology, Incorporated, 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 Logistic Center Canada, Arthrex Manufacturing Inc., Arthrex Mexico, S.A. de C.V. and 3 more
Establishment registrations 1220246, 3002579136, 3006990600, 3010331645, 3011230048, 3013700547, 3014004349, 3014262693, 3015231789, 3015974593, 3016851379, 3019269298, 3020704423, 3027339877, 3030926959
FEI numbers 1220246, 3002579136, 3006990600, 3010331645, 3011230048, 3013700547, 3014004349, 3014262693, 3015231789, 3015974593, 3016851379, 3019269298, 3020704423, 3027339877, 3030926959
Establishment operations Contract Manufacturer, Contract Sterilizer, Foreign Exporter, Specification Developer
Registration valid through 2026

At a glance

  • 10–99 Registered establishments listing this device
  • 1–9 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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