RIGEL 3DR Standalone Anterior Cervical Interbody Fusion System

FDA registration

MIRUS, LLC·1 product·🇺🇸 United States

RIGEL™ 3DR Standalone Anterior Cervical Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Integrated Fixation, Cervical

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Cervical

CoRoent

FDA UDI

Nuvasive, Inc.·00887517570468·CoRoent Ant TLIF Ti, 13x12x34mm 8°

CONVERGE RETI-LOCK MULTI-HOLE REINFORCEMENT CUP

FDA registration

Sterigenics US, LLC·4 products·🇺🇸 United States

External Remote Controller ERC 4P

FDA registration

NuVasive Specialized Orthopedics, Inc.·4 products·🇺🇸 United States

Ophthalmic Knife

FDA UDI

KATENA PRODUCTS, INC.·00841668113370·CLEAR CORNEA KNIFE 3.2MM (BX/5)

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·1 product·🇺🇸 United States

IconiX

FDA registration

X-NAV TECHNOLOGIES, LLC.·2 products·🇺🇸 United States

FREEPRINT splintmaster taff 1000g

FDA registration

DETAX GMBH·2 products·🇩🇪 Germany

3D Printing Material Splint

FDA registration

AIDITE (QINHUANGDAO) TECHNOLOGY CO., LTD·2 products·🇨🇳 China

CONVERGE RETI-LOCK MULTI-HOLE REINFORCEMENT CUP

FDA 510(k)

FDA Class 2 ·Orthopedic

TEPHAFLEX BRAIDED SUTURE

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Suture, Recombinant Technology

FDA classification

FDA Class 2 ·Suture, Recombinant Technology

Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

FDA classification

FDA Class 2 ·Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented