D186172

FDA registration

STERITECH, INC.·2 products·🇺🇸 United States

5MM CUFF ANCHOR

FDA registration

STRYKER ENDOSCOPY·2 products·🇺🇸 United States

3910-100-010

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

5MM CUFF ANCHOR

FDA registration

STRYKER EMEA Supply Chain Services·2 products·🇳🇱 Netherlands

STRYKER WEDGE SUTURE ANCHOR

FDA 510(k)

FDA Class 2 ·Orthopedic

ENDOSKELETON® TA nanoLOCK® Surface Technology

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·5 products·🇺🇸 United States

Endoskeleton® TCS Interbody Fusion Device

FDA registration

Sterigenics US, LLC·5 products·🇺🇸 United States

ENDOSKELETON® TA nanoLOCK® Surface Technology

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·5 products·🇺🇸 United States

Spectro2/30 Pulse Oximeter

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

ENDOSKELETON® TA nanoLOCK® Surface Technology

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·5 products·🇮🇳 India

ENDOSKELETON® TA nanoLOCK® Surface Technology

FDA registration

Titan Spine, a Division of Medtronic·5 products·🇺🇸 United States

Spectro2/30 Pulse Oximeter

FDA registration

ICU Medical, Inc.·1 product·🇺🇸 United States

IMAGEN PARAINFLUENZA GROUP

FDA registration

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

IMAGEN PARAINFLUENZA GROUP

FDA registration

REMEL EUROPE LTD·1 product·🇬🇧 United Kingdom

Administration Sets and Accessories

FDA registration

Sterigenics Radiation Technologies, LLC·1 product·🇺🇸 United States

BCI WW1030 PULSE OXIMETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Endoskeleton® TA Interbody Fusion Device, Endoskeleton® TAS Interbody Fusion Device, Endoskeleton® TO Interbody Fusion Device, Endoskeleton® TT Interbody Fusion Device, Endoskeleton® TC Interbody Fusion Device, Endoskeleton® TCS Interbody Fusion Device, Endoskeleton® TL Interbody Fusion Device, Endoskeleton® TA Vertebral Body Replacement (VBR) Device

FDA 510(k)

FDA Class 2 ·Orthopedic

Fastener, Fixation, Nondegradable, Soft Tissue

FDA classification

FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

Oximeter

FDA classification

FDA Class 2 ·Oximeter