15 results · 22ms · Sources: EU EUDAMED, US FDA

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AQUACEL AG FOAM HYDROFIBER FOAM DRESSING WITH SILVER, ADHESIVE AND NON ADHESIVE

FDA 510(k)
FDA Unclassified ·Unknown

MICROVISION SCLERAL BUCKLING COMPONENTS

FDA 510(k)
FDA Class 2 ·Ophthalmic

LIL-LETS SILK COMFORT COMPACT, PLASTIC APPLICATOR, LITE, REGULAR, SUPER, SUPER PLUS AND ULTRA LIL-LETS NON APPLICATOR,

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

INTELLAMAP ORION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·April 15, 2025

ROD, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

TRIATHLON P/A CR BEADED #5L

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MBH·January 29, 2024

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 22, 2013

PARADIGM INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 26, 2014

MAVERICK2 BALLOON CATHETER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LOX·June 14, 2011

INTELLAMAP ORION?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·January 30, 2026

TRIATHION

FDA Adverse Event
Injury ·HOWMEDICA OSTEONICS CORP.·Product code JWH·December 14, 2023

INTELLAMAP ORION

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·November 21, 2024

TRIATHION COMPONENT

FDA Adverse Event
Injury ·HOWMEDICA OSTEONICS CORP.·Product code JWH·December 14, 2023

INTELLAMAP ORION?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·February 26, 2026

INTELLAMAP ORION

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRF·December 12, 2024