29 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BioPhotas Celluma3
FDA 510(k)
FDA Class 2
·Physical Medicine
CoRoent
FDA UDI
Nuvasive, Inc.·00887517566393·CoRoent Ant TLIF PEEK, 15x12x28mm 0°
Epimed
FDA UDI
EPIMED INTERNATIONAL, INC·00818788020406·22g TW x 8.0" Chiba Style Needle w/ Introducer
FILTERWIRE EZ EMBOLIC PROTECTION SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
STRAUMANN CARES SCREW-RETAINED BRIDGE TITANIUM, STRAUMANN CARES DOLDER BAR TITANIUM
FDA 510(k)
FDA Class 2
·Dental
ANTHEM RF
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014
SCANNER TAG
FDA Adverse Event
Malfunction
·SURGICOUNT·Product code LWH·July 2, 2011
SECURA DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 7, 2013
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·December 26, 2019
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·July 19, 2019
PTA BALLOON CATHETER(OHICHO3)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·December 13, 2017
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 14, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·September 30, 2020
BD CONNECTA¿ 3-WAY STOPCOCK
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·September 12, 2023
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 31, 2025