10 results
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29ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Marrow Cellution Bone Marrow Aspiration Needle
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HNM Women Care
FDA UDI
HNM STAINLESS, LLC.·00812171029069·PESSARY, OVAL #4, W/SUPPORT, 2.75”
EKOS PERIPHERAL INFUSION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
GEON RAPID DIGITAL THERMOMETER MODEL: MT-B117, MT-B127, MT-B130, MT-B132FA
FDA 510(k)
FDA Class 2
·General Hospital
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·June 6, 2013
STEALTHSTATION TREON TREATMENT GUIDANCE SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC.·Product code HAW·June 22, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008
ROD CUTTER
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXZ·July 31, 2023
TORNIER PERFORM ANATOMIC AUG MED RIGHT GLENOID 15 DG
FDA Adverse Event
Injury
·TORNIER INC·Product code KWS·March 8, 2024
Medtronic MiniMed(TM) Mio(TM) (MMT-921, 921T, 923, 923T, 925, 925T, 941, 941T, 943, 943T, 945, 945T, 961, 963, 963T, 965, 965T, 975, 975T)
FDA Enforcement
Class II
·Ongoing·Medtronic Inc.·November 29, 2017