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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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107 records meeting your search criteria returned- Product Code: MJO Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CENTINEL SPINE, LLC. INFERIOR END PLATE MEDIUM 0-STERILE 03/12/2021
CENTINEL SPINE, LLC. PRODISC L US IMPLANT INFERIOR ENDPLATE 02/05/2021
CENTINEL SPINE, LLC. PRODISC L US IMPLANT SUPERIOR ENDPLATE 02/05/2021
CENTINEL SPINE, LLC. PRODISC L US IMPLANT PE INLAY W/ TANTALU 02/05/2021
ZIMMER BIOMET SPINE INC. MOBI-C IMPLANT 15X19 H5 US 09/14/2020
LDR MÉDICAL UNKNOWN MOBI-C IMPLANT 09/08/2020
LDR MEDICAL MOBI-C IMPLANT, UNKNOWN SIZE 09/12/2019
CENTINEL SPINE, LLC. PRODISC L TOTAL DISC REPLACEMENT DEVICE 08/29/2019
CENTINEL SPINE, LLC. PRODISC L TOTAL DISC REPLACEMENT DEVICE 08/29/2019
CENTINEL SPINE, LLC. PRODISC L TOTAL DISC REPLACEMENT DEVICE 08/29/2019
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