17 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2
FDA 510(k)
FDA Class 2
·Anesthesiology
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613017705·K-Wire, Double Ended, Trocar Point, Diameter Si...
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741720450·
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788020499·20g TW x 4.5" Coudé® Blunt Nerve Block Needle w...
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674172045060·
ONCONTROL BONE MARROW BIOPSY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DIMENSION VISA HBA1C, MODEL K3105A
FDA 510(k)
FDA Class 2
·Hematology
TRULIANT PS CEM FEM PS CEM RIGHT SZ 4.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 15, 2024
AQUILEX FLUID CONTROL SYSTEM
FDA Adverse Event
Malfunction
·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·March 12, 2020
PINNACLE MTL INS NEUT36IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 17, 2012
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 17, 2012
PINNACLE MTL INS NEUT36IDX56OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 19, 2012
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·November 17, 2012
HEARTMATE II LVAS
FDA Adverse Event
Other
·THORATEC CORP.·Product code DSQ·October 10, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 10, 2013
HUMAPEN ERGO, BURGUNDY/CLEAR
FDA Adverse Event
Malfunction
·ELI LILLY AND COMPANY·Product code FMF·September 17, 2008
TRU CC FEMORAL SIZE 1 LEFT
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·October 15, 2025