FDA device listing

Shoulder joint metal/ polymer semi-constrained cemented prosthesis,Univers Revers Shoulder Prosthesis System

FDA device listing 1772694788 · ARTHREX, INC.

Key facts

Proprietary names Shoulder joint metal/ polymer semi-constrained cemented prosthesis,Univers Revers Shoulder Prosthesis System
Owner/operator ARTHREX, INC.
Owner/operator number 1220287
Premarket submissions K142863
Product codes PHX
Device names PHX - Shoulder Prosthesis, Reverse Configuration
Device class Class II
Classification regulations (21 CFR) 888.3660
Review panels Orthopedic
Registered establishments Arthrex Australia Pty Ltd., Arthrex Distribution Hub EMEA B.V., Arthrex GmbH, Arthrex, Inc., ARTHREX, INC., Arthrex Japan G.K. (Shinjuku), Arthrex Logistic Center, Arthrex Manufacturing Inc., Arthrex New Zealand Limited, Arthrex (Shanghai) Co., Ltd., Arthrex Singapore Pte Ltd.
Establishment registrations 1220246, 3002579136, 3009423112, 3010331645, 3012470322, 3014004349, 3014262693, 3015231789, 3016851379, 3019269298, 3020704423
FEI numbers 1220246, 3002579136, 3009423112, 3010331645, 3012470322, 3014004349, 3014262693, 3015231789, 3016851379, 3019269298, 3020704423
Establishment operations Contract Manufacturer, Contract Sterilizer, Foreign Exporter, Manufacturer, 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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