27 results · 27ms · Sources: EU EUDAMED, US FDA

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UNIFUSE Infusion System with Cooper Wire

FDA 510(k)
FDA Class 2 ·Cardiovascular

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113356·CLEAR CORNEA KNIFE 2.8MM (BX/5)

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113370·CLEAR CORNEA KNIFE 3.2MM (BX/5)

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113363·CLEAR CORNEA KNIFE 3.0MM (BX/5)

NOBELACTIVE TIULTRA NP 3.5X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

NOBELACTIVE TIULTRA NP 3.5X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

COOLTOUCH II

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

MEDTEXX GREEN COLOUR POWDERED NITRILE RUBBER EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

TROCHANTERIC NAIL KIT, TI GAMMA3 11X180MM X 125

FDA Adverse Event
Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 1, 2012

PARIETEX UGYTEX PP 15X10CM XL

FDA Adverse Event
Injury ·SOFRADIM PRODUCTION·Product code FTL·June 21, 2013

INSPIRAL

FDA Adverse Event
Other ·MEDTECH PRODUCTS LTD.·Product code HIS·October 12, 2008

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

SYSTEM, APPENDAGE CLOSURE, LEFT ATRIAL

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·July 15, 2025

FLEXCATH ADVANCE STEERABLE SHEATH

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·April 4, 2023

ARCTIC FRONT ADVANCE® CARDIAC CRYOABLATION CATHETER

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·April 4, 2023

ARCTIC FRONT ADVANCE® CARDIAC CRYOABLATION CATHETER

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·April 4, 2023

ACHIEVE MAPPING CATHETER - 20 MM

FDA Adverse Event
Injury ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code DRF·April 4, 2023

HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

FDA Adverse Event
Injury ·HEARTWARE, INC.·Product code DSQ·November 15, 2023

HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

FDA Adverse Event
Injury ·HEARTWARE, INC.·Product code DSQ·April 15, 2025

HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

FDA Adverse Event
Injury ·HEARTWARE, INC.·Product code DSQ·June 5, 2023