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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
ARTHROCARE CORPORATION UNKNOWN COBLATION DEVICE 01/30/2024
SOLTA MEDICAL, INC. THERMAGE FLX (TG-3A) AND ACCESSORIES 01/24/2024
ALMA LASERS LTD OPUS COLIBIRI 01/22/2024
COVIDIEN MFG DC BOULDER LIGASURE 01/11/2024
MODERN MEDICAL EQUIP MFG LTD SUCTION COAG, F/S, 10FR, 25/CS 01/11/2024
ETHICON ENDO-SURGERY, LLC. EES GENERATOR 01/10/2024
MAQUET CARDIOVASCULAR LLC VASOVIEW HEMOPRO 01/09/2024
CONSOLIDATED MEDICAL EQUIPMENT COMPANY ADVANCED ENERGY GENERATOR 01/09/2024
CONSOLIDATED MEDICAL EQUIPMENT COMPANY ADVANCED ENERGY GENERATOR 01/09/2024
CONSOLIDATED MEDICAL EQUIPMENT COMPANY ADVANCED ENERGY GENERATOR 01/09/2024
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