7,315 results · 42ms · 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.

K-Grip (KFORCE Grip), K-Push (KFORCE Muscle Controller), K-Pull (KFORCE Link), K-Move (KFORCE Sens), K-Bubble (KFORCE Bu

FDA registration
KINVENT HELLAS·1 product·🇬🇷 Greece

TST X Tissue Stainer

FDA registration
MEDITE MEDICAL GMBH·1 product·🇩🇪 Germany

IPL Therapy Machine

FDA registration
BEIJING ADSS DEVELOPMENT CO., LTD.·1 product·🇨🇳 China

eSteth

FDA registration
TECH4LIFE ENTERPRISES CANADA INC·1 product·🇨🇦 Canada

USERAPID Decalcifying Solution, USEDECALC Decalcifying Solution

FDA registration
MEDITE MEDICAL GMBH·1 product·🇩🇪 Germany

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·BLAZER II, BLAZER II HTD, BLAZER PRIME HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·BLAZER II, BLAZER II HTD, BLAZER PRIME HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·Blazer II, Blazer II HTD, Blazer Prime HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·BLAZER II, BLAZER II HTD, BLAZER PRIME HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·BLAZER PRIME HTD, BLAZER II, BLAZER II HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·BLAZER II, BLAZER II HTD,BLAZER PRIME HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·Blazer II, Blazer II HTD, Blazer Prime HTD

Cardiac Ablation Percutaneous Catheter

FDA Pre-Market Approval
FDA Class 3 ·Blazer II, Blazer II HTD, Blazer Prime HTD

LIAISON® 1-84 PTH Assay

FDA UDI
Diasorin Inc.·08056771600125·

Device, Thermal Ablation, Endometrial

FDA Pre-Market Approval
FDA Class 3 ·HTA SYSTEM

Device, Thermal Ablation, Endometrial

FDA Pre-Market Approval
FDA Class 3 ·HTA SYSTEM

Device, Thermal Ablation, Endometrial

FDA Pre-Market Approval
FDA Class 3 ·HTA SYSTEM

Device, Thermal Ablation, Endometrial

FDA Pre-Market Approval
FDA Class 3 ·HTA SYSTEM

Device, Thermal Ablation, Endometrial

FDA Pre-Market Approval
FDA Class 3 ·HTA SYSTEM

Dental Zirconia Blank & Dental Zirconia Pre-Shaded Blank

FDA registration
CHANGSHA HONCHON TECHNOLOGY CO., LTD·1 product·🇨🇳 China