22 results · 41ms · Sources: EU EUDAMED, US FDA

Harrier

FDA registration
Choice Spine·2 products·🇺🇸 United States

CULVER TOOL & ENGINEERING

FDA registration
CULVER TOOL & ENGINEERING·2 products·🇺🇸 United States

Choice Spine Lumbar Spacer System (Sabre™, Shark™, Hornet™, Harpoon™), Choice Spine Interbody Fusion System (Harrier™), Choice Spine Vertebral Body Replacement System (Hawkeye™)

FDA 510(k)
FDA Class 2 ·Orthopedic

DYNAMIC COMPRESSION SMA Staple System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074051444·STAPLE 8162103 3MM X 9MM TWO PRONG SMA

Mouthpiece, Disposable Flex, 3/4" OD, 2.625" L

FDA UDI
A-M SYSTEMS, LLC·00817081023534·Mouthpiece, Disposable Flex, 3/4" OD, 2.625" L

Peerless Buccal Tube

FDA UDI
ORMCO CORPORATION·00889989054095·PRLS 2NDMOL B/T 12DEG -10T 022 NDX UL

Skeletal Dynamics Sterilization Trays

FDA registration
SKELETAL DYNAMICS, INC·1 product·🇺🇸 United States

DARCO Force Compression Screw

FDA registration
HG Medical GmbH·1 product·🇩🇪 Germany

DC4124 DARCO® HEADLESS COMPRESSION SCREW 3.2MM X 24MM

FDA registration
Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia

DARCO

FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

Viant AS&O Holdings, LLC

FDA registration
Viant AS&O Holdings, LLC·1 product·🇺🇸 United States

DARCO

FDA registration
WRIGHT MEDICAL TECHNOLOGY, INC.·1 product·🇺🇸 United States

DC4124 DARCO® HEADLESS COMPRESSION SCREW 3.2MM X 24MM

FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

KERRISON PUNCH RONGEUR

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896018280·KERRISON PUNCH RONGEUR UP-ANGLE TIP

Stealth System S300

FDA registration
CARDIAC INSIGHT, INC.·2 products·🇺🇸 United States

AL.CHI.MI.A. SRL

FDA registration
AL.CHI.MI.A. SRL·1 product·🇮🇹 Italy

XenMatrix

FDA registration
DAVOL INC., SUB. C.R. BARD, INC.·3 products·🇺🇸 United States

SKELETAL DYNAMICS STERILIZATION TRAYS

FDA 510(k)
FDA Class 2 ·General Hospital

DARCO FORCE TITANIUM COMPRESSION SCREW

FDA 510(k)
FDA Class 2 ·Orthopedic

Intervertebral Fusion Device With Bone Graft, Lumbar

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