18 results · 49ms · Sources: EU EUDAMED, US FDA

C&A Tool Engineering, Inc. Auburn Plant

FDA registration
C&A Tool Engineering, Inc. Auburn Plant·1 product·🇺🇸 United States

SURGICAL INSTRUMENT MANUFACTURERS, LLC

FDA registration
SURGICAL INSTRUMENT MANUFACTURERS, LLC·2 products·🇺🇸 United States

SPIRA Open Matrix ALIF and LLIF

FDA registration
FRIEDRICH DANIELS GMBH·2 products·🇩🇪 Germany

SPIRA-O Open Matrix OLIF

FDA registration
CAMBER SPINE TECHNOLOGIES·2 products·🇺🇸 United States

ODP - Intervertebral fusion device with bone graft, cervical

FDA registration
FLEX-CELL PRECISION, INC.·2 products·🇺🇸 United States

SPIRA Open Matrix ALIF and LLIF

FDA 510(k)
FDA Class 2 ·Orthopedic

Oticon

FDA UDI
Oticon A/S·05707131338976·SIYA 1, BTE 13 PP 2.4G 105 C090

Catheter, Percutaneous

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

VISIGI 3D

FDA registration
BOEHRINGER LABORATORIES, LLC·1 product·🇺🇸 United States

Pump Assembly w/ Private

FDA registration
PLAXTRON INDUSTRIAL (M) SDN. BHD.·1 product·🇲🇾 Malaysia

VAMED MEDICAL INSTRUMENT CO.,LTD, Foshan, Guangdong, CHINA

FDA registration
VAMED MEDICAL INSTRUMENT CO.,LTD·1 product·🇨🇳 China

Sterigenics US LLC

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

Dental Barriers and Sleeves

FDA registration
BH Medical Products Co., Ltd·1 product·🇨🇳 China

MODIFIED HD GUIDE CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

SURSIGNS VS2 VITAL SIGNS MONITOR, SURESIGNS VS3 VITAL SIGNS MONITOR, SURESIGNS VM SERIES PATIENT MONITORS

FDA 510(k)
FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification
FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Electrocardiograph

FDA classification
FDA Class 2 ·Electrocardiograph

Catheter, Percutaneous

FDA classification
FDA Class 2 ·Catheter, Percutaneous