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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
CELESTICA DE MONTERREY S.A. DE C.V. ENDO GIA 08/12/2022
US SURGICAL PUERTO RICO ENDO GIA 08/10/2022
US SURGICAL PUERTO RICO UNKNOWN ENDO GIA INSTRUMENT 08/10/2022
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 07/29/2022
US SURGICAL PUERTO RICO ENDO GIA ULTRA 07/29/2022
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 07/29/2022
COVIDIEN LP LLC NORTH HAVEN SIGNIA 07/29/2022
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 07/26/2022
US SURGICAL PUERTO RICO ENDO GIA ULTRA 07/26/2022
COVIDIEN LP LLC NORTH HAVEN SIGNIA 07/14/2022
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