137 results · 21ms · Sources: EU EUDAMED, US FDA

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RK EPIDURAL NEEDLE

FDA 510(k)
FDA Class 2 ·Anesthesiology

Vial Adaptor

FDA UDI
WEST PHARMA. SERVICES IL, . LTD·07290108240450·VA 20mm ML VF-USA

Cook

FDA UDI
COOK INCORPORATED·00827002141773·Fascial Dilator

Paltop

FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108692389·Conical 5mm Straight Ball Abutment Ti

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0120050·Screw Sizing Block

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197175197·Coakley Curettes Fig. 5 170mm,...

OsteoMed

FDA UDI
OSTEOMED LLC·00845694034654·MFx Instrumentation Tray 3

MODIFICATION TO ALARMVIEW WIRELESS DATA NETWORK SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

BOLUSPRO ULTRA

FDA 510(k)
FDA Class 2 ·Radiology

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018

IAB : 8 FR - 40 CC

FDA Adverse Event
Injury ·ARROW INTERNATIONAL, INC.·Product code DSP·July 29, 2005

NAIL, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES SELZACH·Product code JDS·February 13, 2017

MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Injury ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·July 14, 2005

UNKNOWN ENDURON LINER

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·August 4, 2005

NIPRO

FDA Adverse Event
Other ·NIPRO MEDICAL CORPORATION.·Product code FIB·August 15, 2005

CONTAK RENEWAL 3

FDA Adverse Event
Death ·CLONMEL·Product code NIK·March 3, 2006

MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·GUIDANT VASCULAR INTERVENTION·Product code MAF·November 1, 2005

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR LTD.·Product code MCM·October 13, 2005

RUGEL (BARD/DAVOL)

FDA Adverse Event
Injury ·DAVOL·Product code FTL·September 14, 2005

IQ MARKER GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC·Product code DQX·August 4, 2005