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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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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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482 records meeting your search criteria returned- Product Code: LXH Product Problem: Bent Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US EXPRESSEW III SUTUER PASSER W/O HOOK 05/24/2018
DEPUY ORTHOPAEDICS INC US SROM DIST STEM TRIAL 9 STD 05/23/2018
DEPUY ORTHOPAEDICS INC US ADAPTER REMOVER INSTRUMENT 05/22/2018
DEPUY MITEK LLC US EXPRESSEW III W/O HOOK 05/20/2018
MEDOS INTERNATIONAL SàRL EXPRESSEW III AC+ GUN 05/19/2018
CONMED CORPORATION SPECTRUM AUTOPASS SUTURE PASSER 05/17/2018
DEPUY ORTHOPAEDICS INC US MBT REVISION T-HANDLE 05/16/2018
DEPUY IRELAND 9616671 SIG HP REV TC3 BOX TRIAL SZ5 05/10/2018
DEPUY IRELAND 9616671 SIG HP REV TC3 BOX TRIAL SZ4 05/10/2018
STRYKER SPINE-US SPECIALTY CANNULATED PROBE 05/03/2018
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