EnSite Array Catheter

FDA registration

MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

EnSite Array Catheter

FDA registration

St. Jude Medical, Cardiology Division, Inc.·1 product·🇺🇸 United States

ENSITE ARRAY MULTI-ELECTRODE DIAGNOSTIC CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Intracardiac Mapping, High-Density Array

FDA classification

FDA Class 2 ·Catheter, Intracardiac Mapping, High-Density Array

WAVELIGHT GmbH

FDA registration

WAVELIGHT GmbH·2 products·🇩🇪 Germany

WAVELIGHT GmbH

FDA registration

WAVELIGHT GmbH·2 products·🇩🇪 Germany

1504 Disposable Set FS200

FDA registration

Sterigenics Belgium Petit Rechain S.A.·2 products·🇧🇪 Belgium

closed incision wound care system CISNaP Kit (CSNA100 & CSNA1005)

FDA registration

Sterigenics U.S. LLC·1 product·🇺🇸 United States

TALOS® HA PEEK IBF

FDA UDI

MEDITECH SPINE, LLC·B167321210060·

TALOS® IBF

FDA UDI

MEDITECH SPINE, LLC·B167311210060·

Invictus

FDA UDI

ALPHATEC SPINE, INC.·00190376240985·AO Quick Connect Axial Handle, Fixed with Jewel...

APIXIA INC.

FDA registration

APIXIA INC.·1 product·🇺🇸 United States

APEX Knee System

FDA UDI

Omni Life Science, Inc.·00841690117810·Stemmed Modular Tibia Tray Trial Size 6

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450383704·

WAVELIGHT FS200 LASER SYSTEM MODEL: FS200

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

STARTOX DRUG OF ABUSE SCREENING TEST

FDA 510(k)

FDA Class 2 ·Clinical Toxicology

PERSONA® Vivacit-E®

FDA UDI

Zimmer, Inc.·00889024469136·

PERSONA® Vivacit-E®

FDA UDI

Zimmer, Inc.·00889024469204·

PERSONA® Vivacit-E®

FDA UDI

Zimmer, Inc.·00889024469174·

PERSONA® Vivacit-E®

FDA UDI

Zimmer, Inc.·00889024469143·