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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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68 records meeting your search criteria returned- Product Code: ONG Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SOLTA MEDICAL, INC CLEAR + BRILLIANT LASER SYSTEM 03/20/2024
SOLTA MEDICAL, INC CLEAR + BRILLIANT TOUCH LASER SYSTEM 01/30/2024
SOLTA MEDICAL, INC CLEAR + BRILLIANT LASER SYSTEM 03/23/2023
SOLTA MEDICAL, INC CLEAR + BRILLIANT LASER SYSTEM 03/03/2023
SOLTA MEDICAL, INC CLEAR + BRILLIANT LASER SYSTEM 10/14/2022
SOLTA MEDICAL, INC CLEAR + BRILLIANT LASER SYSTEM 02/17/2022
SOLTA MEDICAL, INC CLEAR + BRILLIANT LASER SYSTEM 07/28/2021
SOLTA MEDICAL INC. FRAXEL RE:STORE LASER SYSTEM 04/20/2021
SOLTA MEDICAL INC. FRAXEL RE:STORE LASER SYSTEM 04/20/2021
SOLTA MEDICAL, INC FRAXEL DUAL 1550/1927 LASER SYSTEM & ACC 03/26/2021
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