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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
AESCULAP AG ACTIV L SUP.PLATE SIZE XL 6°/SPIKES 01/12/2022
AESCULAP AG ACTIV L PE-INLAY 8.5MM 01/11/2022
AESCULAP AG ACTIV L INF.PLATE S1 SIZE XL 5°/SPIKES 01/11/2022
AESCULAP AG ACTIV L PE-INLAY 8.5MM 12/29/2021
AESCULAP AG ACTIV L SUP.PLATE SIZE M 11°/SPIKES 12/29/2021
AESCULAP AG ACTIV L INF.PLATE SIZE M 0°/SPIKES 12/29/2021
LDR MÉDICAL MOBI-C IMPLANT M"STANDARD" 13X15 H5 12/22/2021
CENTINEL SPINE, LLC. PRODISC L US INFERIOR ENDPLATE MEDIUM 0 06/04/2021
CENTINEL SPINE, LLC. PRODISC L US SUPERIOR ENDPLATE MEDIUM 11 06/04/2021
CENTINEL SPINE, LLC. PRODISC L US PE-INLAY W/ X-RAY MARKER, S 06/04/2021
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