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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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65 records meeting your search criteria returned- Product Code: HRX Product Problem: Failure to Power Up Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SMITH & NEPHEW, INC. DII CONTROLLER 02/05/2024
ARTHREX, INC. DW ARTHROSCOPY FLUID MANAGEMENT DEV 01/30/2024
ARTHREX, INC. DW ARTHROSCOPY FLUID MANAGEMENT DEV 12/28/2023
ARTHREX, INC. DW ARTHROSCOPY FLUID MANAGEMENT DEV 12/08/2023
ARTHREX, INC. DW ARTHROSCOPY FLUID MANAGEMENT DEV 10/12/2023
STRYKER ENDOSCOPY-SAN JOSE PKG, CROSSFLOW CONSOLE 06/21/2023
DEPUY MITEK LLC US MICRO TORNADO HP W HANDCONTROL 02/09/2022
SMITH & NEPHEW, INC. DII CONTROLLER 12/10/2021
SMITH & NEPHEW, INC. SERVICE REPL CAMERA HEAD LENS INT SYS 06/18/2021
ARTHREX, INC. DW ARTHROSCOPY FLUID MANAGEMENT DEV 11/16/2020
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