PacePro Wire

FDA registration

OPSENS INC.·2 products·🇨🇦 Canada

PacePro Wire

FDA 510(k)

FDA Class 2 ·Cardiovascular

VERTE-STACK® Spinal System

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994305183·IMPLANT 6240864 ANATOMIC 16X14X8MM

ANATOMIC PEEK CERVICAL FUSION SYSTEM

FDA UDI

MEDTRONIC SOFAMOR DANEK, INC.·00613994366443·IMPLANT 4240864 ANATOMIC C 16X14X 8MM

Anatomic PEEK™ Cervical Fusion System with Nanotechnology

FDA UDI

NANOVIS SPINE, LLC·00814216028150·ANATOMIC PEEK w/ Nano 16 x 14 x 8 x 4.6°

Velofix Interbody Fusion System

FDA registration

CG MedTech USA, Inc.·2 products·🇺🇸 United States

AESCULAP, INC.

FDA registration

AESCULAP, INC.·1 product·🇺🇸 United States

Velofix Interbody Fusion System

FDA registration

CG MedTech Co., Ltd.·2 products·🇰🇷 South Korea

AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

EchoGo Amyloidosis (1)

FDA registration

ULTROMICS, LTD.·1 product·🇬🇧 United Kingdom

NovaLine SP-C35 Transducer Protector

FDA registration

BAIN MEDICAL EQUIPMENT(GUANGZHOU) CO., LTD.·1 product·🇨🇳 China

Accelerate Arc™ system

FDA registration

ACCELERATE DIAGNOSTICS, INC.·1 product·🇺🇸 United States

CRANIOFIX AND CRANIOFIX2 TITANIUM CLAMP SYSTEM

FDA 510(k)

FDA Class 2 ·Neurology

VELOXTM INTERBODY FUSION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Wire, Guide, Catheter

FDA classification

FDA Class 2 ·Wire, Guide, Catheter

Plate, Cranioplasty, Preformed, Non-Alterable

FDA classification

FDA Class 2 ·Plate, Cranioplasty, Preformed, Non-Alterable

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Cervical