CARESTREAM DRX-EVOLUTION PLUS

FDA registration

Carestream Health, Inc·1 product·🇺🇸 United States

DRX-EVOLUTION, MODEL VX3733-SYS

FDA 510(k)

FDA Class 2 ·Radiology

SFAM-Surgiform

FDA registration

Eurofins Infinity Laboratory Group Inc.·1 product·🇺🇸 United States

Synergy Health Ireland Ltd

FDA registration

Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland

SFAM 3-D

FDA registration

SURGICAL TECHNOLOGY LABORATORIES INC.·1 product·🇺🇸 United States

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

NG-Test CARBA 5

FDA registration

NG BIOTECH·1 product·🇫🇷 France

QUALITY TECH SERVICES, LLC

FDA registration

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

SURGIFORM AUGMENTATION MATERIAL (S.F.A.M.)

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

ULTRA -THIN SDS BALLOON DILATATION CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

System, X-Ray, Stationary

FDA classification

FDA Class 2 ·System, X-Ray, Stationary

Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

FDA classification

FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous