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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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Super Search Devices@FDA
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
MEDTRONIC, INC. CAPSURE® Z NOVUS 03/31/2023
BIOTRONIK SE & CO. KG ELOX P 53 BP 02/27/2023
BIOTRONIK SE & CO. KG ELOX P 53 BP 02/14/2023
OSCOR INC. FLEXION PERMANENT PACING LEAD 10/25/2022
BIOTRONIK SE & CO. KG PX 45 JBP 03/24/2022
OSCOR INC. FLEXION PERMANENT PACING LEAD 12/22/2021
OSCOR INC. PY PERMANENT PACING LEAD 11/30/2021
BIOTRONIK SE & CO. KG SX 60/15 BP 11/03/2021
OSCOR INC. RX PERMANENT PACING LEAD 11/01/2021
OSCOR INC. ELAPASS PJ 752 10/19/2021
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