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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
COVIDIEN MANSFIELD TRUCLEAR 12/14/2023
HOLOGIC, INC MYOSURE REACH TISSUE REMOVAL DEVICE 12/14/2023
GYRUS ACMI, INC. CUTTING LOOP (12/PK) 12/14/2023
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR 12/14/2023
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR 12/14/2023
SHIRAKAWA OLYMPUS CO., LTD. VISERA HYSTEROVIDEOSCOPE 12/14/2023
OLYMPUS WINTER & IBE GMBH RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR 12/13/2023
GYRUS ACMI, INC. SEAL KIT, 6-12FR, 12/BOX 12/12/2023
SHIRAKAWA OLYMPUS CO., LTD. OES HYSTEROFIBERSCOPE 12/12/2023
OLYMPUS WINTER & IBE GMBH TELESCOPE, 70°, 4 MM 12/12/2023
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