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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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95 records meeting your search criteria returned- Product Code: MJO Product Problem: Malposition of Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
LDR MÉDICAL MOBI-C IMPLANT 15X17 H5 US 02/28/2018
LDR MÉDICAL MOBI-C IMPLANT 15X17 H5 US 02/28/2018
GLOBUS MEDICAL INC. SECURE C 02/05/2018
LDR MÉDICAL MOBI-C IMPLANT 13X17 H5 US 11/28/2017
LDR MÉDICAL MOBI-C P&F US 09/22/2017
LDR MÉDICAL MOBI-C IMPLANT 13X17 H5 US 09/22/2017
LDR MÉDICAL MOBI-C IMPLANT 13X15 H5 US 09/13/2017
WARSAW ORTHOPEDICS PRESTIGE CERVICAL DISC SYSTEM 08/08/2017
WARSAW ORTHOPEDICS PRESTIGE CERVICAL DISC SYSTEM 08/04/2017
DEPUY SYNTHES SPINE DISCOVER ARTIFICIAL DISC 05/15/2017
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