733 results · 31ms · 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.

Follicle Clarity

FDA 510(k)
FDA Class 2 ·Radiology

OsteoMed

FDA UDI
OSTEOMED LLC·00845694019781·FPS 2.0mm x 12mm Standard Screw

ARKEO, Wedge Fixation System

FDA UDI
Auxano Medical LLC·00850055649798·ARKEO Evan's Wedge, 20x20x12

Thino Roth Bracket, .022, Mini Size, UL2

FDA UDI
Astar Orthodontics Inc.·06941673501460·

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193100654·EVOS Straight HA PEEK, 12mm x 8mm x 22mm, Flat ...

OsteoMed

FDA UDI
OSTEOMED LLC·00845694073745·FPS 2.0 x 12mm Screw Sterile Qty 5

NON-STERILE, POWDER-FREE BLUE, NITRILE EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

ECG HOME

FDA 510(k)
FDA Class 2 ·Cardiovascular

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·March 1, 2012

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·February 24, 2012

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·March 1, 2012

INVACARE MEDICAL

FDA Adverse Event
Other ·DANYANG JUMAO HEALTHCARE EQUIPMENT CO.,LTD.·Product code IOR·October 26, 2012

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 29, 2014

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·August 15, 2011

CANE, CRUTCH AND WALKER TIPS AND PADS

FDA Adverse Event
UNKNOWN·Product code INP·July 8, 2013

HEARTSTREAM FR2

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·March 29, 2012

IVS TUNNELLER

FDA Adverse Event
Injury ·BALLYMONEY - USS·Product code FTL·September 21, 2012

ASPHERE M SPEC 12/14 36 +5

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·August 22, 2012

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM INC.·Product code MDS·March 28, 2014

ORCHESTRA

FDA Adverse Event
Malfunction ·SORIN CRM S.R.L.·Product code KRG·December 21, 2012