20 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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IPS E. MAX PRESS ABUTMENT SOLUTIONS FOR NOBEL BIOCARE
FDA 510(k)
FDA Class 2
·Dental
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193112442·HA PEEK EVOS Straight, ,8mmx10mmx 22mm , BICONV...
3DP Lumbar Interbody System
FDA UDI
Genesys Orthopedics Systems LLC·M719GL3DL1240080·Large 8-Degree 3DP LLIF - 12mm x 40mm
Sochi
FDA UDI
Altus Spine, LLC·00843210166582·Polyaxial Screw, 4.0mm x 8mm
Phadia 2500+ LAS Connector
FDA UDI
Phadia AB·07333066021621·Phadia 2500+ LAS Connector
Atoll™
FDA UDI
Seaspine Orthopedics Corporation·10889981052478·4.0mm x 8mm Poly Screw Assm. The Atoll OCT Spin...
SMALL BARD VENTRALEX PATCH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MEDLINE HIGH PRESSURE INJECTION TUBING
FDA 510(k)
FDA Class 2
·Cardiovascular
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237322·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237346·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237377·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237353·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237384·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237391·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237339·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024237360·
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP.·Product code NIQ·February 27, 2006
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 17, 2013
ASKU
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DTB·June 14, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 2, 2015