29 results · 26ms · 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.

SENSITITRE 18-24 HOURS SUSCEPTIBILITY PLATES (QUINUPRISTIN/DALFOPRISTIN)

FDA 510(k)
FDA Class 2 ·Microbiology

TruForm

FDA UDI
Rmo, Inc.·00885797100016·MN 1MOL BD KT STD NO/L R&L 218

TruForm

FDA UDI
Rmo, Inc.·00885797099709·MX MLR BDS R/L SE ASIA ASST100

artVeneer life

FDA UDI
Merz Dental GmbH·D7092001558·artVeneer life lower anteriors, UIL, BL1

X-Series Size 1 Vertical Bitewing YELLOW Bite Block 3-Pack

FDA UDI
CLIKTECH LLC·00856200001558·X-Series Size 1 Vertical Bitewing YELLOW Bite B...

AUDIOSCREENER OAE + ABR

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

SYNTHES (USA) WRIST FUSION PLATES (WFP)

FDA 510(k)
FDA Class 2 ·Orthopedic

CARDIOSAVE HYBRID, TYPE I PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·February 17, 2026

CARDIOSAVE

FDA Adverse Event
Malfunction ·DATASCOPE CORP·Product code DSP·April 17, 2014

CARDIOSAVE

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·September 3, 2014

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·July 22, 2024

CARDIOSAVE HYBRID TYPE D PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·November 20, 2025

CARDIOSAVE HYBRID TYPE D PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·January 29, 2026

CARDIOSAVE HYBRID TYPE D PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·April 2, 2026

CARDIOSAVE HYBRID TYPE D PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·December 18, 2025

CARDIOSAVE HYBRID, 3.1 EDITION

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·December 24, 2025

FOUNDATION KNEE

FDA Adverse Event
ENCORE MEDICAL, L.P.·Product code JWH·March 13, 2013

VANGUARD DCM PS TIBIAL BEARING 12MM X 71/75MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·February 25, 2011

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·February 21, 2008

CARDIOSAVE HYBRID, TYPE I PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·November 27, 2025