23 results
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26ms
·
Sources: EU EUDAMED, US FDA
HAMID HOOK ATTACHMENT DEVICE FOR HEMILAMINECTOMY RETRACTOR
FDA 510(k)
FDA Class 2
·Neurology
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665586155·MIS Cannulated Screw M, Ø5.0 x 40mm, Ø5.5mm Rod
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117629·Augment Trial Size 4
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937187·Percutaneous Transluminal Angioplasty Balloon C...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690126539·Augment Trial Size 4
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955938351·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939525·Percutaneous Transluminal Angioplasty Balloon C...
TELEPULSE
FDA 510(k)
FDA Class 2
·Anesthesiology
ALGINATE FIBER
FDA 510(k)
FDA Unclassified
·Unknown
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024206595·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024206588·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024206571·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024206618·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024206564·
NexGen® Legacy®
FDA UDI
Zimmer, Inc.·00889024206601·
NexGen®
FDA UDI
Zimmer, Inc.·00889024206557·
AEQUALIS REVERSED STERILE PIN 200 MM
FDA Adverse Event
Injury
·TORNIER S.A.S.·Product code JDW·July 24, 2015
ASR UNI FEMORAL IMPL SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 6, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 18, 2014
ALPS MIS DRILL GUIDE LK 2.7MM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code HRS·January 19, 2018