10,000 results · 61ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Clariti 1 day

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Bausch + Lomb (Kalifilcon A) Soft Contact Lens

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Dailies Total 1 90 PACK

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Acuvue Vita for astigmatism

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

PROCLEAR 1 DAY 90 PACKS

FDA registration
LENS GLOBAL Limited·1 product·🇬🇧 United Kingdom

FRESH LOOK 1 DAY

FDA registration
LENS GLOBAL Limited·1 product·🇬🇧 United Kingdom

AIR OPTIX Hydraglyde

FDA registration
LENS GLOBAL Limited·1 product·🇬🇧 United Kingdom

Acuvue Oasys Max 1 Day Multifocal

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Acuvue Oasys With Transition

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Focus Dailies

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

THOR LX2

FDA registration
THOR Photomedicine Ltd·1 product·🇬🇧 United Kingdom

SENSEI V2 (Reusable Probe) System

FDA registration
Lightpoint Surgical Limited·1 product·🇬🇧 United Kingdom

Acuvue Oasys for Astigmatism

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Dailies total 1 multifocal

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Newfoundland Fecal Occult Blood Self-test

FDA registration
NEWFOUNDLAND DIAGNOSTICS·1 product·🇬🇧 United Kingdom

Newfoundland UTI Self-test

FDA registration
NEWFOUNDLAND DIAGNOSTICS·2 products·🇬🇧 United Kingdom

Newfoundland Cholesterol Self-test

FDA registration
NEWFOUNDLAND DIAGNOSTICS·1 product·🇬🇧 United Kingdom

Proclear 1 day

FDA registration
LENS GLOBAL Limited·2 products·🇬🇧 United Kingdom

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·Senza HFX iQ System (model IPG3000)

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·IntellaNav MiFi Open-Irrigated (OI) Ablation Catheter