444 results · 22ms · Sources: EU EUDAMED, US FDA

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Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·Roadsaver/CASPER Carotid Stent Device

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·Roadsaver/CASPER Carotid Stent Device

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 11, 2025

CASPER 5F

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 24, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 21, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 21, 2025

CASPER 5F

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·April 1, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 28, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 24, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 23, 2025

CASPER 5F

FDA Adverse Event
Injury ·MICROVENTION INC.·Product code NIM·February 22, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 23, 2025

CASPER X 5F

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 22, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION, INC.·Product code NIM·February 21, 2025

CASPER X

FDA Adverse Event
Injury ·MICROVENTION INC.·Product code NIM·February 22, 2025

MaXcess

FDA UDI
Nuvasive, Inc.·00887517184467·MaXcess Blade, Light Cable Adapter

AMPLITUDE

FDA UDI
AMPLITUDE SAS·03701089500814·Resurfacing Patellar Implant NM Cemented Ø 30 mm

LEONE SPA

FDA UDI
LEONE SPA·08033707080817·THREE-JAW PLIERS CLASSIX

APEX Spine System

FDA UDI
SPINECRAFT, LLC·00193082014765·APEX Ti Poly Screw Dia.10.0, 30mm

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869621151·MOSS VRS Ti rod, Ø5.5x30mm, curved