86 results · 23ms · 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.

MOSS MIAMI 6.35MM ROD SYSTEM PEDICLE AND LAMINAR HOOKS

FDA 510(k)
FDA Class 2 ·Orthopedic

MPS

FDA UDI
QUEST MEDICAL INC·00634624501157·MPS® Additive Agent Cassette

artVeneer life

FDA UDI
Merz Dental GmbH·D7092001105·artVeneer life upper anteriors, BS, A35

TruFlex™

FDA UDI
Ortho Organizers, Inc.·00190707126520·TRUFLEX NiTi Thermal Euro Upper 020 (10pk)

TruFlex

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730013835·NiTi Thermal Euro Upper 020 10 archwires per pack

PRCT2

FDA UDI
FX SOLUTIONS·03701037307588·PRCT II TRIAL HUMERAL PLATE LEFT 5 HOLES

UNIVERSAL PLUS/FLOVAC

FDA UDI
Conmed Corporation·30653405011402·UNIVERSAL PLUS/FLOVAC, SUMP CANNULA WITHOUT SID...

FlowLogic Variety Kit

FDA UDI
SONENDO, INC.·00810209421403·FlowLogic Variable Deep Dive Kit, 21mm 00810209...

MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),

FDA 510(k)
FDA Class 2 ·Neurology

WAKO HDL-C/LDL-C CALIBRATOR

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

0008020776-2025-001105

FDA Adverse Event
Injury ·ANTHOGYR SAS·Product code DZE·November 10, 2025

MALE LL ADAPTOR

FDA Adverse Event
Malfunction ·Product code FPA·June 17, 2021

INJECTOR LUER LOCK N35J

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·August 11, 2020

MALE LL ADAPTOR

FDA Adverse Event
Malfunction ·Product code FPA·June 18, 2021

IMPAX CV REPORTING

FDA Adverse Event
Malfunction ·AGFA HEALTHCARE CORP·Product code LLZ·February 26, 2013

TRAPEZOID RX LITHOTRIPTER COMPATIBLE BASKET, MODELS 1086, 1087, 1088

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code LQC·February 24, 2011

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·February 14, 2008

KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and positioning of tissue to be removed in the patient's body, enabling improved surgical precision and patient safety.

FDA Enforcement
Class II ·Ongoing·Klinika Mdical Gmb·May 21, 2025

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·December 1, 2010

OT ULTRA METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 10, 2011