69 results · 23ms · Sources: EU EUDAMED, US FDA

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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