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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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120 records meeting your search criteria returned- Product Code: KWL Product Problem: Break Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ACTIS RETAINING STEM INSERTER 12/05/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 6 11/20/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 6 11/19/2019
DEPUY ORTHOPAEDICS INC US ACTIS BROACH SZ 5 11/19/2019
DEPUY ORTHOPAEDICS, INC. ACTIS (HIP) 11/12/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 9 11/07/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 8 11/06/2019
DEPUY IRELAND - 9616671 ACTIS RETAINING STEM INSERTER 11/04/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 6 10/08/2019
DEPUY IRELAND 9616671 ACTIS BROACH SZ 4 07/30/2019
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