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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
 

 
 
6 records meeting your search criteria returned- Product Code: EFB Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
LARES RESEARCH LARES RESEARCH 10/25/2021
NAKANISHI INC. NSK 04/27/2020
NAKANISHI INC. NSK 02/11/2020
KAVO DENTAL / KALTENBACH & VOIGT LUX M05L 01/30/2020
KAVO DO BRASIL INDUSTRIA E COMERCIO LTDA HENRY SCHEIN MAXIMA PRO 45 N/O FIXED END 07/16/2019
NAKANISHI INC. NSK 07/02/2019
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