23 results · 53ms · Sources: EU EUDAMED, US FDA

Repris Bladder Injection System

FDA registration
URO1 MEDICAL, INC.·1 product·🇺🇸 United States

Repris Bladder Injection System

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Endoscopic Injection Needle, Gastroenterology-Urology

FDA classification
FDA Class 2 ·Endoscopic Injection Needle, Gastroenterology-Urology

Responsive Orthopedics Total Knee Arthroplasty System

FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973106913·TRIAL 90-SRK-180214 POLY PS 2X14MM

BALANCE MICROPLASTY HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304446366·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694034203·Profile Zero 25mm Gap Plate

K010214 Urological Catheter

FDA registration
Sterigenics US LLC·1 product·🇺🇸 United States

Synergy Health Daniken AG

FDA registration
Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

CORNERSTONEPSR Spinal System

FDA registration
Medtronic Engineering and Innovation Center (MEIC)·1 product·🇮🇳 India

K010214 Urological Catheter

FDA registration
Sterigenics US, LLC·1 product·🇺🇸 United States

QUALITY TECH SERVICES, LLC

FDA registration
QUALITY TECH SERVICES, LLC·1 product·🇺🇸 United States

STERIS ISOMEDIX PUERTO RICO, INC.

FDA registration
STERIS ISOMEDIX PUERTO RICO, INC.·1 product·🇺🇸 United States

Synergy Health Allershausen GmbH

FDA registration
Synergy Health Allershausen GmbH·1 product·🇩🇪 Germany

CORNERSTONEPSR Spinal System

FDA registration
MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH·1 product·🇩🇪 Germany

CORNERSTONEPSR Spinal System

FDA registration
MEDTRONIC PUERTO RICO OPERATIONS CO., HUMACAO·1 product·🇺🇸 United States

CORNERSTONEPSR Spinal System

FDA registration
MEDTRONIC SOFAMOR DANEK USA, INC.·1 product·🇺🇸 United States

VESTEX

FDA registration
VXK Products, LLC·1 product·🇺🇸 United States

Gold Standard Diagnostics Borrelia Burgdorferi Igg/Igm ELISA Test Kit

FDA registration
Gold Standard Diagnostics Frankfurt GmbH·1 product·🇩🇪 Germany

OsteoMed

FDA UDI
OSTEOMED LLC·00845694065887·Profile 0 25 Gap Plate Sterile Qty 2

CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic