15 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GENESYS SPINE ANTERIOR BUTTRESS PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
COE® Adhesive
FDA UDI
Gc America Inc.·D6581339111·COE® ADHESIVE BOTTLE ONLY, 13mL
COE® Adhesive
FDA UDI
Gc America Inc.·10386040004985·COE® ADHESIVE BOTTLE ONLY, 13mL
SENOMARK ULTRA BREAST TISSUE MARKER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RAPIDCROSS PTA RAPID EXCHANGE BALLOON DILATATION CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
WAVEWRITER ALPHA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 20, 2024
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 2, 2014
SALTO TALARIS
FDA Adverse Event
Injury
·TORNIER SAS·Product code HSN·May 23, 2013
MARISA
FDA Adverse Event
Injury
·ARJO MED AB LTD·Product code FSA·June 15, 2011
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·May 21, 2024
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·April 17, 2024
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER (ISRAEL) LTD.·Product code DQK·December 22, 2016
CARTO® 3 SYSTEM
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code DQK·January 10, 2024