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

Clinical Screw Omnigrip

FDA registration
NOBEL BIOCARE DISTRIBUTION CENTER BV·1 product·🇳🇱 Netherlands

Clinical Screw Omnigrip

FDA registration
NOBEL BIOCARE AB, PRODUKTION·1 product·🇸🇪 Sweden

NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium

FDA registration
INFINIA DENTAL LAB·1 product·🇺🇸 United States

Clinical Screw Omnigrip

FDA registration
Nobel Biocare Services AG·1 product·🇨🇭 Switzerland

Clinical Screw Omnigrip

FDA registration
NOBEL BIOCARE AB·1 product·🇸🇪 Sweden

Clinical Screw Omnigrip

FDA registration
NOBEL BIOCARE PROCERA, LLC·1 product·🇺🇸 United States

NobelProcera Titanium ASC Abutment, Omnigrip Clinical Screw Titanium

FDA 510(k)
FDA Class 2 ·Dental

Boston Scientific Limited

FDA registration
Boston Scientific Limited·1 product·🇮🇪 Ireland

BOSTON SCIENTIFIC CORPORATION

FDA registration
BOSTON SCIENTIFIC CORPORATION·1 product·🇨🇷 Costa Rica

Synergy Health Ireland Ltd

FDA registration
Synergy Health Ireland Ltd·1 product·🇮🇪 Ireland

Boston Scientific Corporation

FDA registration
Boston Scientific Corporation·1 product·🇺🇸 United States

Boston Scientific Corporation

FDA registration
Boston Scientific Corporation·1 product·🇺🇸 United States

Boston Scientific Limited

FDA registration
Boston Scientific Limited·1 product·🇮🇪 Ireland

Boston Scientific Corporation

FDA registration
Boston Scientific Corporation·1 product·🇺🇸 United States

Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System

FDA registration
TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.·3 products·🇹🇼 Taiwan

Boston Scientific Corporation

FDA registration
Boston Scientific Corporation·1 product·🇺🇸 United States

Suzhou Zhenwu Medical Co., Ltd.

FDA registration
Suzhou Zhenwu Medical Co., Ltd.·1 product·🇨🇳 China

Prodigy Pressure Activated Safety Lancet

FDA registration
PRODIGY DIABETES CARE, LLC·1 product·🇺🇸 United States

Philips IntelliSite Pathology Solution 5.1

FDA registration
Philips Electronics Ltd·1 product·🇨🇦 Canada

INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular