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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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76 records meeting your search criteria returned- Product Code: LFL Product Problem: Failure to Power Up Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ETHICON ENDO-SURGERY, LLC. ULTRACISION** HARMONIC SCALPEL** HAND PI 08/18/2016
ETHICON ENDO-SURGERY, LLC. ULTRACISION HARMONIC ACE 08/04/2016
ETHICON ENDO-SURGERY, LLC. ULTRACISION HARMONIC ACE 08/04/2016
COVIDIEN, FORMERLY US SURGICAL A DIVISON AUTOSONIX* ULTRA SHEARS* 5MM INSTRUMENT 06/16/2016
COVIDIEN LLC (SHANGHAI) LIGASURE ATLAS HANDSWITCHING 37CM 05/05/2016
ETHICON ENDO-SURGERY, LLC. ULTRACISION HARMONIC ACE 04/28/2016
ETHICON ENDO-SURGERY, LLC. ULTRACISION** HARMONIC SCALPEL** HAND PI 03/25/2016
OLYMPUS MEDICAL SYSTEMS CORP. ULTRASONIC SURGICAL SYSTEM SONOSURG 02/29/2016
SOUND SURGICAL TECHNOLOGIES, LLC VASER AMPLIFIER 02/26/2016
OLYMPUS MEDICAL SYSTEMS CORP. ULTRASONIC SURGICAL SYSTEM SONOSURG 01/09/2016
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