28 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

FRONTIER ANTERIOR SCOLIOSIS SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450329962·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134496·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134359·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134335·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134410·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134519·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134458·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134373·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134397·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134472·

READERS.COM

FDA UDI
FGX INTERNATIONAL INC.·00192304134434·

SURGI-VISION PROSTATE COIL

FDA 510(k)
FDA Class 2 ·Radiology

PTW DOSIMETRY DIODE, T60008

FDA 510(k)
FDA Class 2 ·Radiology

WATCHPAT100

FDA Adverse Event
Injury ·ITAMAR MEDICAL LTD.·Product code MNR·November 12, 2007

AC POWER MODULE

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 25, 2013

ANIMAS INSULIN CARTRIDGE

FDA Adverse Event
Malfunction ·ANIMAS CORP.·Product code LZG·March 4, 2011

ASCENSIA CONTOUR

FDA Adverse Event
Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·March 11, 2008

INSET

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 2, 2025

INSET

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·December 2, 2025