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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
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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 MEDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 03/01/2024
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 03/01/2024
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD 15X15 H5 US 12/20/2023
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 11/17/2023
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD 13X17 H5 US 11/10/2023
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD 13X17 H5 US 11/10/2023
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 11/03/2023
LDR MEDICAL MOBI-C IMPLANT "M" STANDARD, UNKNOWN SIZ 11/03/2023
LDR MEDICAL MOBI-C IMPLANT 13X15 H5 US 07/25/2023
CENTINEL SPINE PRODISC C US IMPLANT MEDIUM-DEEP 5MM 05/03/2023
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