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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: MNI Product Problem: Defective Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
OSSEUS FUSION SYSTEMS, LLC. BLACK DIAMOND PEDICLE SCREW 08/05/2022
MEDOS INTERNATIONAL SÀRL VIPER 04/02/2020
GS MEDICAL CO, LTD GSS 09/22/2017
GS MEDICAL CO, LTD GSS 07/12/2017
STRYKER SPINE-SWITZERLAND XIA 3 TITANIUM BLOCKER 12/19/2016
STRYKER SPINE-SWITZERLAND XIA 3 TITANIUM BLOCKER 12/19/2016
STRYKER SPINE-SWITZERLAND XIA 3 TITANIUM POLYAXIAL SCREW DIA 6.0 X 11/09/2016
STRYKER SPINE-SWITZERLAND XIA LP POLYAXIAL SCREW 6.5 X 40MM 09/23/2016
AESCULAP AG & CO. KG S4C SET SCREW NEW VERSION 08/13/2015
AESCULAP AG S4C SET SCREW NEW VERSION 07/30/2015
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