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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience(MAUDE)

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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
IRIDEX CORPORATION MICROPULSE P3 DEVICE 08/08/2024
ALMA LASERS LTD HARMONY XL PRO 08/06/2024
ALMA LASERS LTD HARMONY XL PRO 07/25/2024
LUMENIS BE LTD STELLAR M22 07/18/2024
CUTERA, INC. ENLIGHTEN III 07/06/2024
CYNOSURE LLC PICOSURE PRO 07/03/2024
LUMENIS LTD MOSES PULSE 06/18/2024
IRIDEX CORPORATION MICROPULSE P3 DEVICE 06/17/2024
IRIDEX CORPORATION Powered laser surgical instrument 06/17/2024
IRIDEX CORPORATION MICROPULSE P3 DEVICE 06/15/2024
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