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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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429 records meeting your search criteria returned- Product Code: KWL Report Date From: 1/1/2019 Report Date To: 12/31/2019
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ManufacturerBrand NameDate Report Received
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 3 12/19/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 5 12/18/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 5 12/17/2019
DEPUY IRELAND - 9616671 ACTIS COLLARED HIGH SIZE 10 12/12/2019
DEPUY ORTHOPAEDICS INC US ACTIS BROACH SZ 3 12/11/2019
DEPUY ORTHOPAEDICS INC US ACTIS BROACH SZ 3 12/11/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 7 12/11/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 3 12/10/2019
DEPUY ORTHOPAEDICS INC US UNKNOWN HIP FEMORAL AUGMENT 12/10/2019
DEPUY IRELAND - 9616671 ACTIS BROACH SZ 5 12/09/2019
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