34 results · 29ms · Sources: EU EUDAMED, US FDA

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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