886 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.

BEGO SEMADOS Tr 58350; BEGO SEMADOS RS/RSX-Line Tray Plus, BEGO Semados Tr 58349; BEGO Semados Tr 58348, BEGO Semados DSTr 58356; Drill Stop Tray Plus (RS/RSX-Line), BEGO SEMADOS PKTr 58357; Prosthetic Kit

FDA 510(k)
FDA Class 2 ·General Hospital

VITA TITANKERAMIK

FDA UDI
Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft·J017B2014120·VITA TITANKERAMIK OPAQUE, D2, 12 g

16PW - Washington Gas - Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588014425·16PW - Washington Gas - Poly White

UP - Vehicle - 380-55230 - 18 Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588014173·UP - Vehicle - 380-55230 - 18 Metal

ABSORBENT PAPER POINTS

FDA UDI
DiaDent Group International·08806383556330·"An absorbent paper points is an endodontic pap...

PM 1800 CONSERVING DEVICE

FDA 510(k)
FDA Class 2 ·Anesthesiology

LATEX EXAMINATION GLOVES, POWDER FREE, POLYMER COATED

FDA 510(k)
FDA Class 1 ·General Hospital

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·January 22, 2015

I-STAT PT/INRCARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code GJS·October 14, 2014

HEARTWARE VENTRICULAR ASSIST SYSTEM

FDA Adverse Event
Malfunction ·HEARTWARE, INC·Product code DSQ·July 19, 2017

TRUETRACK

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·February 5, 2015

CAPSURE SP NOVUS LEAD

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO VILLALBA·Product code DTB·September 23, 2025

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·December 24, 2014

OT ULTRALINK METER

FDA Adverse Event
Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

CAPSUREFIX

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2011

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 26, 2013

TRUE RESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·March 19, 2015

HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

FDA Adverse Event
Malfunction ·HEARTWARE, INC.·Product code DSQ·February 15, 2018

ISOLINE

FDA Adverse Event
Injury ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code MRM·March 3, 2016

HEARTWARE VENTRICULAR ASSIST SYSTEM-CONTROLLER 2.0

FDA Adverse Event
Malfunction ·HEARTWARE, INC.·Product code DSQ·February 13, 2018