23 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ViewPoint 6
FDA 510(k)
FDA Class 2
·Radiology
SpheRx
FDA UDI
Nuvasive, Inc.·00887517443984·SpheRx® II Conn, 30mm Transverse Fixed
CoRoent
FDA UDI
Nuvasive, Inc.·00887517570895·CoRoent Ant TLIF Ti, 14x11x30mm 0°
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704265705·
LCP
FDA UDI
Synthes GmbH·10886982166678·3.5MM LCP® POSTEROLATERAL DISTAL HUMERUS PLATE ...
Pomee
FDA UDI
POMEE CORPORATION·G15772413000·Rochester pean forceps 5 1/2" straight
Integra® Miltex®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780160113·Integra® Miltex® DeBakey-Semb Ligature Carrier 11"
2.4MM TMS SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036061821·
JOBST Elvarex
FDA UDI
BSN-Jobst GmbH·04019702404104·Elvarex 2/Thigh High/Closed Toe, E-Version, Kne...
X-CUBE 90
FDA 510(k)
FDA Class 2
·Radiology
Airway Mobilescope
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
TRUSTEEL
FDA Adverse Event
Malfunction
·Product code FPA·December 7, 2021
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·January 7, 2020
ANGIO-SEAL STS PLUS DEVICE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code MGB·November 20, 2008
HUDSON CIRCUIT, NEONATAL, DUAL HTD LUMB W/18 IN
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BZO·August 19, 2011
ATLANTIS? SR PRO²
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·July 22, 2013
Covidien/ Mallinckrodt CT9000, CT9000 ADV (J-Bow component 241300), contrast media delivery system for diagnostic imaging.
FDA Recall
Terminated
·Mallinckrodt Inc·Product code DXT·April 14, 2008
OT ULTRA MINI METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE GMBH·Product code NBW·November 28, 2019
OT ULTRA MINI METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE GMBH·Product code NBW·November 28, 2019
PORTEX NRFIT CONNECTOR EPIDURAL MINIPAK
FDA Adverse Event
Malfunction
·SMITHS MEDICAL CZECH REPUBLIC A. S·Product code CAZ·February 7, 2025