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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
 

 
 
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18 records meeting your search criteria returned- Product Code: NUH Report Date From: 1/1/2018 Report Date To: 12/31/2018
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ManufacturerBrand NameDate Report Received
SANOFI AVENTIS U.S. LLC ICY HOT SMARTRELIEF TENS THERAPY BACK ST 12/26/2018
BAYER HEALTHCARE LLC, CONSUMER CARE ALEVE DIRECT THERAPY TENS 11/21/2018
BAYER HEALTHCARE LLC, CONSUMER CARE ALEVE TENS DEVICE DIRECT THERAPY UNIT 10/26/2018
BAYER HEALTHCARE LLC, CONSUMER CARE ALEVE TENS DEVICE DIRECT THERAPY UNIT 08/24/2018
BAYER HEALTHCARE LLC, CONSUMER CARE ALEVE DIRECT THERAPY TENS 08/06/2018
HOLLYWOG, LLC WITOUCH PRO 07/10/2018
ACTEGY LTD REVITIVE DX 05/31/2018
ACTEGY LTD REVITIVE MEDIC 05/31/2018
ACTEGY LTD CBV3 05/30/2018
ACTEGY LTD REVITIVE MEDIC 2469MD 05/30/2018
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