27 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROLONG, MODELS PL50, PL100, PL150
FDA 510(k)
FDA Class 2
·Anesthesiology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040054571·Polycarbonate Crowns
Essential Kit
FDA UDI
MEDIVATORS INC.·40677964010741·Essential Kit includes DEFENDO Valves, Basin, B...
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001129·artVeneer life lower anteriors, UIL, A35
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167900011290·
CURE LP
FDA UDI
MEDITECH SPINE, LLC·B167S1900011290·
CURE LP
FDA UDI
SpineArt SA·07640270060729·LATERAL LUMBAR PLATE L29
ROVERS ENDOCERVEX-BRUSH
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
GEIGER NEEDLE ADAPTER, MODEL 406
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CS100 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·March 11, 2025
ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·January 17, 2019
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·February 19, 2026
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·September 2, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·September 2, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 2, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 2, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·July 2, 2025
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·March 15, 2026
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013
QUANTUM 2 SYSTEM
FDA Adverse Event
Other
·ARTHROCARE CORPORATION·Product code GEI·February 18, 2011