INTEGRATE-C

FDA registration

HAPPE SPINE·1 product·🇺🇸 United States

INTEGRATE-C Interbody Fusion System

FDA registration

REVELATION MEDICAL DEVICES, LLC·1 product·🇺🇸 United States

INTEGRATE -C Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

MyoSPECT

FDA registration

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING·1 product·🇮🇱 Israel

Inline Sensor Assembly and

FDA registration

Bioptimal International Pte. Ltd.·1 product·🇸🇬 Singapore

Inline Sensor Assembly and

FDA registration

BIOXIN MEDICAL CO., LTD·1 product·🇨🇳 China

MyoSPECT

FDA registration

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING·1 product·🇮🇱 Israel

MyoSPECT

FDA registration

GE Medical Systems Israel, Functional Imaging·1 product·🇮🇱 Israel

SANTORINI™ Corpectomy Cage System

FDA UDI

K2M, INC.·10888857020955·Solid Cage

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776165970·Freeman Petite Face Lift Retractor W

18M - Five Star Safety - w/Logo

FDA UDI

Certified Safety Manufacturing, Inc.·00766588620046·18M - Five Star Safety - w/Logo

Arthrex (Shanghai) Co., Ltd.

FDA registration

Arthrex (Shanghai) Co., Ltd.·4 products·🇨🇳 China

Irreversible Electroporation Probe

FDA registration

JIANA STERILIZATION TECHNOLOGY (HANGZHOU) CO., LTD·1 product·🇨🇳 China

DS-W

FDA registration

BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.·2 products·🇨🇳 China

Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe

FDA registration

ZHEJIANG CURAWAY MEDICAL TECHNOLOGY CO., LTD·1 product·🇨🇳 China

CARDIAC OUTPUT KIT, MODEL CO-1 & INLINE SENSOR CABLE, MODEL ILS-1

FDA 510(k)

FDA Class 2 ·Cardiovascular

MyoSPECT, MyoSpect ES

FDA 510(k)

FDA Class 2 ·Radiology

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

PERSONA® Vivacit-E®

FDA UDI

Zimmer, Inc.·00889024242968·

PERSONA® Vivacit-E®

FDA UDI

Zimmer, Inc.·00889024243019·