21 results · 27ms · 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.

AMSURE DISPOSABLE SYRINGE WITH/WITHOUT NEEDLE

FDA 510(k)
FDA Class 2 ·General Hospital

Mini-Sprint®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70610391·Mini Sprint-Brackets 5-5 McLaugh/Benn/Trev. .01...

THE IMPLEX HEDROCEL MODULAR ELLIPTICAL ACETABULAR CUP

FDA 510(k)
FDA Class 2 ·Orthopedic

OMNILINK .018 BILIARY STENT SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SCR BIORCI-HA 9X30 STERILE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code MAI·November 13, 2017

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

SCR BIORCI-HA 7X30 7MM HEAD STERILE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code HWC·June 20, 2017

ST JOSEPHS PHOENIX, AZ 1

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

RU NOVOSIBRIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

CP87170 DE MUENCHEN

FDA Adverse Event
Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

2520274-2013-01993

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·April 16, 2013

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCUL

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 13, 2008

ENTERALITE INFINITY ENTERAL FEEDING PUMP

FDA Adverse Event
Other ·MOOG MEDICAL DEVICES GROUP·Product code LZH·April 4, 2011

BIORCI SCRW 8MM X 20MM STRL

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code HWC·January 4, 2018

CP87641 GB SOUTHAMPTON

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DWE·March 22, 2010

SCR BIORCI-HA 7X25 7MM HEAD STERILE

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code HWC·July 29, 2020

SCR BIORCI-HA 9X30 STERILE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code HWC·December 11, 2018

D 100 PH.I.S.I.O. NEWBORN HOLLOW FIBER MEMBRANE OXYGENATOR WITH RESERVOIR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code DTZ·March 28, 2017

ENCOREANYWHERE

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·February 17, 2016