69 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·FINEVISION HP Trifocal IOLs
SpheRx
FDA UDI
Nuvasive, Inc.·00887517440662·SpheRx II Screwdriver, Polyaxial
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925032804·SHEA PARASOL VENT TUBE 1.5 MM I.D. SILICONE
LCP
FDA UDI
Synthes GmbH·10886982164476·4.5MM LCP PROXIMAL TIBIA PLATE 6 HOLES/118MM-RIGHT
PIRANHA
FDA UDI
SPINAL ELEMENTS·00840916112295·2-L CERV PLATE-38mm
Clear Moves Aligners
FDA 510(k)
FDA Class 2
·Dental
Trilogy®
FDA UDI
Zimmer, Inc.·00889024119277·
GMK SPHERE TOTAL KNEE SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·February 11, 2025
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·AbsorbaSeal 5.6.7F Vascular Closure Device
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT CAROTID STENT SYSTEM
MAQUET HCU20
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DWC·November 3, 2014
ISOFLEX P
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·September 8, 2011
AVAULTA SOLO SYNTHETIC SUPPORT SYSTEM - POSTERIOR
FDA Adverse Event
Injury
·BARD SHANNON LTD·Product code FTL·July 18, 2013
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT® Carotid Stent System
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT Carotid Stent System
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT CAROTID STENT SYSTEM
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT Carotid Stent System
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT CAROTID STENT SYSTEM
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT CAROTID STENT SYSTEM
Stent, Carotid
FDA Pre-Market Approval
FDA Class 3
·XACT CAROTID STENT SYSTEM