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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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11 records meeting your search criteria returned- Product Code: KWS Product Problem: Device Inoperable Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
STRYKER GMBH SR 4MM OFFSET HUMERAL HE AD TRIAL 52X23 06/21/2018
STRYKER GMBH BASEPLATE CENTERING GUID E RIGHT 03/26/2018
STRYKER GMBH UNKNOWN REVERSE SHOULDER SCREW 05/25/2017
STRYKER GMBH UNKNOWN REVERSE SHOULDER HUMERAL CUP 05/25/2017
EXACTECH, INC REVERSE TORQUE DEFINING SCREW ASSEMBLY 10/24/2016
EXACTECH, INC EQUINOXE HUMERAL STEM, PRIMARY, PRESS-FI 10/24/2016
ENCORE MEDICAL, L.P. TURON SHOULDER 11/20/2015
ENCORE MEDICAL, L.P. TURON SHOULDER 07/23/2015
ENCORE MEDICAL, L.P. TURON SHOULDER 06/30/2015
ENCORE MEDICAL, L.P. FOUNDATION SHOULDER 12/15/2014
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