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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
SPINAL ELEMENTS, INC OVERWATCH 11/30/2022
MEDOS INTERNATIONAL SàRL CH EXP 6.35 COCR ROD W/HEX ENDS 4 11/30/2022
SEASPINE ORTHOPEDICS CORPORATION MARINER PEDICLE SCREW SYSTEM 11/23/2022
NUVASIVE INC. NUVASIVE RELINE SYSTEM 11/15/2022
ULRICH GMBH & CO. KG UCENTUM 11/11/2022
ULRICH GMBH & CO. KG UCENTUM 11/11/2022
SEASPINE ORTHOPEDICS CORPORATION MARINER PEDICLE SCREW SYSTEM 11/09/2022
AESCULAP AG ENNOVATE POLYAX.SCREW 7.5X45MM CANULATED 11/09/2022
SYNTHES GMBH UNK - CONSTRUCTS: SYNAPSE 10/17/2022
MEDOS INTERNATIONAL SàRL CH UNK - CONSTRUCTS: VIPER 10/17/2022
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