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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
 

 
 
3 records meeting your search criteria returned- Product Code: EJF Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
UNKNOWN PALATAL EXPANDER 05/18/2023
SDS DE MEXICO U1L DAMON Q2 .022 STD TQ 05/01/2023
DYNAFLEX NORRIS 20/26 BRACKET 11/08/2022
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