38 results · 19ms · Sources: EU EUDAMED, US FDA

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ACCESS SEQUESTRATION SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

Zirlux

FDA UDI
HENRY SCHEIN, INC.·H65890124060·Zirlux Shading Liquid - Effects, purple, 30ml

TREK

FDA UDI
ABBOTT VASCULAR INC.·08717648154065·TREK Coronary Dilatation Catheter 2.75 mm x 20 ...

TREK

FDA UDI
ABBOTT VASCULAR INC.·08717648154058·TREK Coronary Dilatation Catheter 2.75 mmx 15 m...

TREK

FDA UDI
ABBOTT VASCULAR INC.·08717648154041·TREK Coronary Dilatation Catheter 2.75 mm x 12 ...

TREK

FDA UDI
ABBOTT VASCULAR INC.·08717648154034·TREK Coronary Dilatation Catheter 2.75 mm x 8 m...

TREK

FDA UDI
ABBOTT VASCULAR INC.·08717648154089·TREK Coronary Dilatation Catheter 2.75 mm x 30 ...

TREK

FDA UDI
ABBOTT VASCULAR INC.·08717648154027·TREK Coronary Dilatation Catheter 2.75 mm x 6 m...

TREK

FDA UDI
ABBOTT VASCULAR INC.·08717648154072·TREK Coronary Dilatation Catheter 2.75 mm x 25 ...

MATIRA ANTERIOR CERVICAL SYSTEM

FDA UDI
Kalitec Direct LLC·B07307K0154061·TRIAL, DRILL GUIDE 14 X 11, 6 MM TA

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00811801036712·Rotating Distractor, 6mm

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 12, 2026

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 12, 2026

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 12, 2026

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 12, 2026

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 12, 2026

INSET II

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 12, 2026

JMS A.V. FISTULA NEEDLE SET WING EATER, MODEL 14G-18G

FDA 510(k)
FDA Class 2 ·General Hospital