13 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TEK-LUBE
FDA 510(k)
FDA Class 1
·Dental
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937934·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955936760·Percutaneous Transluminal Angioplasty Balloon C...
NA
FDA UDI
Biedermann Motech GmbH & Co. KG·04250869657655·MOSS XT Ti Pedicle Screw Ø5.0x80mm light blue, ...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939105·Percutaneous Transluminal Angioplasty Balloon C...
Pulmoguard
FDA UDI
S D I DIAGNOSTICS INC·B279S297925080·Pulmonary Function Test Filter
CONTINUUM KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MED-WEST DUAL LUMEN INTERNAL JUGULAR CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
XMAX MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code ERL·March 31, 2015
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 5, 2014
OLYMPUS SINGLE USE CHANNEL CLEANING BRUSH
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FDX·November 23, 2010
Newton Wire Guide
FDA Enforcement
Class II
·Terminated·Cook Inc.·March 21, 2018