29 results · 22ms · 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.

mCare® Powder Free Nitrile Black Examination Glove

FDA 510(k)
FDA Class 1 ·General Hospital

OsteoMed

FDA UDI
OSTEOMED LLC·00845694015516·2.4mm x 44mm Cannulated Lag Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694070966·Cannulated 2.4 x 44mm Lag Screw Sterile Qty 2

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

ANATOMIC PEEK CERVICAL FUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

TACTICATH

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL·Product code OAE·January 11, 2016

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·October 17, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·November 9, 2018

ROSA ONE

FDA Adverse Event
Injury ·MEDTECH SA·Product code HAW·January 11, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code NAY·January 21, 2019

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code HAW·December 21, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

BARD WOUND DRAIN

FDA Adverse Event
Injury ·C.R. BARD, INC.·Product code GBX·October 7, 2008

NORMALLY CLOSED CHECK VALVE/ANTISIPHON VALVE

FDA Adverse Event
Malfunction ·B. BRAUN MEDICAL, INC.·Product code FPA·June 19, 2013

AP LRG W/RAPIDPORT EZ

FDA Adverse Event
Injury ·ALLERGAN·Product code LTI·July 26, 2011

ROSA ONE

FDA Adverse Event
Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018