38 results · 24ms · 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.

EliA Rib-P

FDA 510(k)
FDA Class 2 ·Immunology

Blade Scalpel

FDA UDI
KATENA PRODUCTS, INC.·00841668113448·SUPER SHARPS 15 DEG 3MM (BX/5)

JMS A.V. FISTULA NEEDLE SET

FDA UDI
JMS SINGAPORE PTE LTD·08888483005833·A.V.FISTULA 15GX1" 30CM W/CLAMP (TWIN)

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668113578·PRESET 600 MICRON KNIFE (BX/5)

EXPERIENCE®

FDA UDI
Gc Orthodontics America Inc.·D78820254000201·EXP MBT 022/U4 UNIV -7T 0A

EXPERIENCE®

FDA UDI
Gc Orthodontics America Inc.·D78820254000441·EXM AND 022/U4&5 UNI -7T 0A 0OF

BIONOSTICS GLUCOSE QUALITY CONTROL SOLUTION FOR USE WITH MEDISENSE BLOOD GLUCOSE TEST STRIP SYSTEMS

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

CARDIO ID+(RZ153+)

FDA 510(k)
FDA Class 2 ·Cardiovascular

AED PRO

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 8, 2008

UNICEL DCX 600I SYNCHRON ACCESS CLINICAL SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code CGZ·August 5, 2011

PROMUS ELEMENT? PLUS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 2, 2013

UNKNOWN ENDO GIA SULU

FDA Adverse Event
Injury ·COVIDIEN SURGICAL·Product code GDW·July 18, 2025

UNKNOWN ENDO GIA SULU

FDA Adverse Event
Death ·COVIDIEN SURGICAL·Product code GDW·July 21, 2025

ENDURANT STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·July 22, 2025

VALIANT STENT GRAFT

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MIH·July 22, 2025

GORE® PRECLUDE® PERICARDIAL MEMBRANE

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code DXZ·February 26, 2026

ARCTIC FRONT ADVANCE® CARDIAC CRYOABLATION CATHETER

FDA Adverse Event
Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·November 5, 2025

SUPERDIMENSION

FDA Adverse Event
Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·August 29, 2025

CROSSCOUNTRY

FDA Adverse Event
Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code EOQ·August 28, 2025

UNKNOWN BIOPSY NEEDLE

FDA Adverse Event
Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code GAA·August 29, 2025