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

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KARL STORZ UDEL Sterilization Trays

FDA 510(k)
FDA Class 2 ·General Hospital

DJO SURGICAL

FDA UDI
Encore Medical, L.P.·00190446943662·SPECIAL, EMPOWR BOX CHISEL, NEBULA STYLE

Disposable Blade

FDA UDI
KATENA PRODUCTS, INC.·00841668113202·BARD-PARKER BLADE #15 PACK OF 50

PLANMED SOPHIE & SOPHIE CLASSIC (WITH DIGISPOT AND CYTOGUIDE)

FDA 510(k)
FDA Class 2 ·Radiology

SYNTHES (USA) MEDIAL DISTAL TIBIA PLATES

FDA 510(k)
FDA Class 2 ·Orthopedic

EMPRINT

FDA Adverse Event
Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code NEY·November 23, 2020

SUPERDIMENSION

FDA Adverse Event
Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·November 30, 2020

GORE® EXCLUDER® AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 20, 2021

TECNIS SYMFONY

FDA Adverse Event
Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·September 10, 2019

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

PROMUS PREMIER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·August 5, 2019

PORT-A-CATH IMPLANTABLE ACCESS SYSTEM

FDA Adverse Event
Injury ·ST PAUL·Product code LJT·August 2, 2023

EON

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 17, 2014

DEPUY PINNACLE ULTAMET

FDA Adverse Event
Injury ·Product code KWA·August 4, 2011

M-1 COT - BASE HIGH LOAD 28

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·July 2, 2013

FLOWFLEX COVID-19 ANTIGEN HOME TEST

FDA Adverse Event
Malfunction ·ACON LABORATORIES, INC.·Product code QKP·June 8, 2023

ENDOSCOPIC LNR CUTR (EXACT CODE UNKNOWN)

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 30, 2025

STARR-EDWARDS SILASTIC BALL HEART VALVE PROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code LWQ·October 31, 2019

EXCOR BLOOD PUMP PU VALVES, 30 ML IN/OUT Ø9 MM

FDA Adverse Event
Malfunction ·BERLIN HEART GMBH·Product code DSQ·April 8, 2019

EVIA DR-T

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·February 25, 2020