BIOLOK SCREW, BIOSTEON SCREW

FDA 510(k)

FDA Class 2 ·Orthopedic

STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT

FDA 510(k)

FDA Class 2 ·Orthopedic

BIOSTEON CROSS PIN

FDA 510(k)

FDA Class 2 ·Orthopedic

LITTLE GRAFTER SCREW

FDA 510(k)

FDA Class 2 ·Orthopedic

GP1 Pro

Basic UDI-DI

EU IVDR · Eu Ivd Class A ·Thermo Electron LED GmbH Zweigniederlassung Osterode·10 devices

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protege RX Carotid Stent Systems and Protege GPS Peripheral Stent Systems

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protégé™ RX Carotid Stent System, Protégé™ GPS™ Self-Expanding Peripheral Stent System

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protégé™ GPS™ Self-Expanding Peripheral Stent System, Protégé™ RX Carotid Stent System

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protégé RX Carotid Stent System; Protégé GPS Self-Expanding Peripheral Stent System

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protégé RX Carotid Stent System; Protégé GPS Self-expanding Peripheral Stent System

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protégé™ RX Carotid Stent System, Protégé™ GPS™ Self-Expanding Peripheral Stent System

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protégé™ RX Carotid Stent System, tégé™ GPS™ Self-Expanding Peripheral Stent System

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Protégé GPS Self-Expanding Peripheral Stent System, Protégé RX Carotid Stent System

ISIGHT

FDA 510(k)

FDA Class 2 ·Ophthalmic

Cursus3

Basic UDI-DI

EU MDR · Eu Md Class 1 ·GPI France·1 device

EMOLIFE

Basic UDI-DI

EU MDR · Eu Md Class 2b ·GPI S.P.A.·1 device

TENGEER

Basic UDI-DI

EU MDR · Eu Md Class 2a ·GPI S.P.A.·1 device

PHEBO

Basic UDI-DI

EU MDR · Eu Md Class 2a ·GPI S.P.A.·1 device

AsTer Total Care

Basic UDI-DI

EU MDR · Eu Md Class 2a ·GPI S.P.A.·1 device

EMONET

Basic UDI-DI

EU MDR · Eu Md Class 2b ·GPI S.P.A.·1 device