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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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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
ETHICON ENDO-SURGERY, LLC. PROXIMATE*RL TITAN HEAVY WIRE 06/07/2018
US SURGICAL PUERTO RICO EEA 06/07/2018
US SURGICAL PUERTO RICO EEA 06/05/2018
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 440MM SHAFT 06/04/2018
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 440MM SHAFT 06/04/2018
ETHICON ENDO-SURGERY, LLC. POWERED 60 ECHELON +, 440MM SHAFT 06/04/2018
US SURGICAL PUERTO RICO ENDO GIA ULTRA 05/25/2018
US SURGICAL PUERTO RICO EEA 05/24/2018
COVIDIEN LP LLC NORTH HAVEN EEA ORVIL 05/23/2018
US SURGICAL PUERTO RICO STAPLE, IMPLANTABLE 05/23/2018
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