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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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361 records meeting your search criteria returned- Product Code: GEI Product Problem: Use of Device Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
JEISYS MEDCAL INC. POTENZA 03/27/2024
INMODE LTD. INMODE RF PRO 03/27/2024
BOVIE MEDICAL CORP. BOVIE MEDICAL 02/23/2024
DEPUY MITEK LLC US VAPR VUE GENERATOR 02/23/2024
DEPUY MITEK LLC US VAPR CLPLSE90 ELECTRODE W HAND CNTRLS 02/20/2024
DEPUY MITEK LLC US VAPR VUE GENERATOR 02/05/2024
CAREFUSION INC. SNOWDEN-PENCER ATRAUMATIC GRASPER 02/02/2024
DEPUY MITEK LLC US VAPR CLPLSE90 ELECTRODE W HAND CNTRLS 01/24/2024
DEPUY MITEK LLC US VAPR VUE WIRELESS FOOTSWITCH 01/22/2024
DEPUY MITEK LLC US VAPR S90 W/ HAND CONTROLS 01/16/2024
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