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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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448 records meeting your search criteria returned- Product Code: MJO Product Problem: Migration or Expulsion of Device Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
LDR MÉDICAL MOBI-C IMPLANT "M" STANDARD 15X17 H5 US 05/04/2018
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PRODISC-C IMPLANT MEDIUM 5MM-STERILE 04/30/2018
LDR MÉDICAL MOBI-C IMPLANT "M" STANDARD 15X15 H5 US 04/05/2018
MEDTRONIC SOFAMOR DANEK PRESTIGE CERVICAL DISC SYSTEM 03/29/2018
WARSAW ORTHOPEDICS PRESTIGE CERVICAL DISC SYSTEM 02/22/2018
WARSAW ORTHOPEDICS PRESTIGE CERVICAL DISC SYSTEM 02/22/2018
LDR MÉDICAL MOBI-C IMPLANT 02/07/2018
LDR MÉDICAL MOBI-C IMPLANT 15X19 H5 US 02/01/2018
WARSAW ORTHOPEDIC, INC PRESTIGE CERVICAL DISC SYSTEM 01/31/2018
LDR MÉDICAL MOBI-C P&F US 01/19/2018
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