20 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Diapaste
FDA 510(k)
FDA Class 2
·Dental
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690127338·Apex Revision Knee System-Revision Tibia Instru...
KMI IMI GROUP
FDA UDI
Innovative Med·00851314007106·Infiltration Cannula
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101063·KNAPP RETRACTOR 4-PRONG SHARP
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690194996·Apex Revision Knee System-Revision Tibia Instru...
R&D INNOVATION PEDICLE SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OLECRANAIL INTRAMEDULLARY FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·October 6, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·March 13, 2026
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·January 13, 2026
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 16, 2014
ALARIS PUMP MODULE
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FRN·June 29, 2011
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
REZUM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·November 18, 2025
NOVOSTITCH PRO MEN RPR SYS 2-0
FDA Adverse Event
Injury
·CETERIX ORTHOPAEDICS, INC·Product code GAT·July 29, 2020