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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 09/17/2021
COVIDIEN MFG DC BOULDER LIGASURE 09/14/2021
ARTHROCARE CORP. TOPAZ EZ IFS 08/09/2021
ARTHROCARE CORP. WEREWOLF FLOW 90 COBLATION WAND 08/05/2021
ARTHROCARE CORP. WEREWOLF FLOW 90 COBLATION WAND 08/01/2021
ARTHROCARE CORP. WEREWOLF FLOW 90 COBLATION WAND 07/22/2021
ARTHROCARE CORP. SIDEWINDER BLADE ICW 07/21/2021
ARTHROCARE CORP. SUPER MULTIVAC 50 ICW 07/09/2021
ARTHROCARE CORP. AMBIENT SUPER MULTIVAC 50 IFS 07/09/2021
ARTHROCARE CORP. FA QUANTUM 2 CONTROLLER 06/30/2021
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