19 results · 23ms · Sources: EU EUDAMED, US FDA

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Bioabsorbable Anchor

FDA 510(k)
FDA Class 2 ·Orthopedic

INDUS TEXTILES TOWEL-STERILE AND NON-STERILE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

JIAJIAN POINTOSELECT DIGITAL

FDA 510(k)
FDA Class 2 ·Neurology

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 7, 2025

TUBE, GASTROINTESTINAL (AND ACCESS)

FDA Adverse Event
Injury ·C. R. BARD INC. (BASD)·Product code KNT·October 28, 2008

ECHELON*FLEX60 ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60 MM

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 17, 2011

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 9, 2013

DEKA SMARTPERIO

FDA Adverse Event
Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code NVK·December 11, 2024

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

SHAFT FOR 90° SCREWDRIVER

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HXX·January 12, 2022

Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Pulse Generator

FDA Enforcement
Class II ·Ongoing·Boston Scientific Corporation·September 25, 2019