"DLP® Aortic Root Cannula with Vent Line

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

DLP Aortic Root Cannula

FDA registration

MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States

DLP Aortic Root Cannula

FDA registration

Medtronic Grand Rapids·1 product·🇺🇸 United States

DLP Cardioplegia Cannula

FDA registration

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

DLP Aortic Root Cannula

FDA registration

Medtronic Mexico S. de R.L. de CV·1 product·🇲🇽 Mexico

DLP Aortic Root Cannula

FDA registration

Medtronic Distribution Center·1 product·🇺🇸 United States

CARDIOPULMINARY BYPASS CATHETER CANNULA

FDA 510(k)

FDA Class 2 ·Cardiovascular

Park Dental Research Corp

FDA registration

Park Dental Research Corp·1 product·🇺🇸 United States

NeuroSight Arc Software

FDA registration

Integra LifeSciences Corporation·1 product·🇺🇸 United States

NeuroSight Arc Software

FDA registration

INTEGRA LIFESCIENCES CORPORATION·1 product·🇺🇸 United States

Medline Integrated Arterial Catheter

FDA registration

CENTURION MEDICAL PRODUCTS, LP·1 product·🇺🇸 United States

OSI O-BALL ABUTMENT HEAD IMPLANTS

FDA 510(k)

FDA Class 2 ·Dental

MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)

FDA 510(k)

FDA Class 2 ·Neurology

Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

FDA classification

FDA Class 2 ·Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Neurological Stereotaxic Instrument

FDA classification

FDA Class 2 ·Neurological Stereotaxic Instrument

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form