19 results · 43ms · Sources: EU EUDAMED, US FDA

Gaitway Implant System

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

GAITWAY IMPLANT SYSTEM, SURGICAL INSTRUMENT SET

FDA 510(k)
FDA Class 2 ·Orthopedic

ArgenZ HT+ 95x18 B1

FDA UDI
ARGEN CORPORATION, THE·D818122738·Dental porcelain/ceramic restoration kit

Durango

FDA registration
DONSON MACHINE COMPANY·4 products·🇺🇸 United States

Highridge Medical, LLC

FDA registration
Highridge Medical, LLC·4 products·🇺🇸 United States

RMS CO.

FDA registration
RMS CO.·4 products·🇺🇸 United States

Olive Branch Distribution Center

FDA registration
Olive Branch Distribution Center·4 products·🇺🇸 United States

LANX FUSION SYSTEM

FDA registration
MICROPULSE INC·4 products·🇺🇸 United States

catheter, percutaneous; catheter, angioplasty, peripheral, transluminal AGILTRAC 35 Peripheral Dilatation Catheter

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

Mendell

FDA registration
Mendell·4 products·🇺🇸 United States

V2F

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

BD Veritor System for Rapid Detection of Group A Strep CLIA waived kit

FDA registration
BECTON, DICKINSON & CO.·1 product·🇺🇸 United States

BD Veritor System for Rapid Detection of Group A Strep CLIA waived kit

FDA registration
BD Rapid Diagnostics (Suzhou) Co. Ltd.·1 product·🇨🇳 China

FORUM Archive and Viewer

FDA registration
CARL ZEISS MEDITEC AG (JENA)·1 product·🇩🇪 Germany

LANX FUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

AGILTRAC .035 PERIPHERAL DILATATION CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

Screw, Fixation, Bone

FDA classification
FDA Class 2 ·Screw, Fixation, Bone

Intervertebral Fusion Device With Integrated Fixation, Lumbar

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar

Catheter, Percutaneous

FDA classification
FDA Class 2 ·Catheter, Percutaneous