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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: INN Product Problem: Use of Device Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ALTIMATE MEDICAL, INC. ACTIVEAID 02/15/2024
ALTIMATE MEDICAL, INC. ACTIVEAID 07/01/2022
ACTIVEAID, LLC ACTIVEAID 10/22/2019
ACTIVEAID, LLC ACTIVEAID 08/07/2019
MAXHEALTH CORP DRIVE MEDICAL 08/31/2016
LA-Z-BOY LA-Z-BOY 08/18/2016
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