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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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9 records meeting your search criteria returned- Product Code: ILY Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
ASA SRL M8 07/28/2021
TOM PALADINO AND SCALARLIGHT / SCALAR LI SCALAR ENGERY 07/27/2021
ASA SRL M6 03/11/2021
MEDX HEALTH CORP MEDX MBM 1100 CONSOLE SYSTEM 09/18/2019
LITECURE LLC LIGHTFORCE 11/10/2017
ASA SRL MPHI 10/26/2017
DJO, LLC CHATTANOOGA 05/10/2017
DJO GLOBAL CHATTANOOGA VECTA GENISYS COLD LASER THE 05/05/2017
LITECURE CLASS IV LASER TREATMENT THE LCT-1000 02/09/2017
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