34 results
·
29ms
·
Sources: EU EUDAMED, US FDA
SLIDESCAN
FDA 510(k)
FDA Class 2
·Hematology
NuVasive
FDA UDI
Nuvasive, Inc.·00887517235800·Universal Broach, 20x22mm
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040015612·Scissor Littauer Jr 5"
artVeneer life
FDA UDI
Merz Dental GmbH·D7092001420·artVeneer life lower anteriors, UBL, C4
Battalion
FDA UDI
ALPHATEC SPINE, INC.·00840967188119·Battalion, LLIF Trial, 0°, 14 mm Wide, 20 mm X ...
PROFESS
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252727057·PROFESS(TM) REGISTRATION KIT
SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003
FDA 510(k)
FDA Class 2
·General Hospital
8100 VITAL SIGNS MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 7, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 9, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 9, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 2, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 2, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 7, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 9, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 9, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 2, 2025
PTERYFIT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·April 2, 2025
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·March 30, 2026
MINMED QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 3, 2024