Plateau-C Titanium

FDA registration

LIFE SPINE·1 product·🇺🇸 United States

Intervertebral fusion device with bone graft, cervical

FDA registration

Acero Precision·1 product·🇺🇸 United States

Plateau-C

FDA registration

ZIBO DANTE CO, LTD·1 product·🇨🇳 China

The Small PLATEAU (PLATEAU-C) Spacer System

FDA 510(k)

FDA Class 2 ·Orthopedic

CG Future Ring

FDA registration

Medtronic Mexico S. de R.L. de CV·1 product·🇲🇽 Mexico

PM50 Patient Monitor

FDA registration

CONTEC MEDICAL SYSTEMS CO., LTD·1 product·🇨🇳 China

CG Future Ring

FDA registration

Medtronic Heart Valves Division·1 product·🇺🇸 United States

BOSS Instruments

FDA UDI

BOSS INSTRUMENTS, LTD., INC.·00888515023338·Bergman-Forester Sponge Fcps, cvd, 9 1/2" (24cm)

3.2-EPR-COL-O EndoRotor® 3.2mm Endoscopic Powered Resection (EPR) Catheter – Colonoscope Short Olympus

FDA registration

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

Arc Synopsis Software

FDA registration

CADWELL INDUSTRIES, INC.·1 product·🇺🇸 United States

Orthocryl®

FDA UDI

DENTAURUM GmbH & Co.KG·J011161127000·Orthocryl® liquid, red/ orthodontic acrylics

PATIENT MONITOR, MODEL PM50

FDA 510(k)

FDA Class 2 ·Cardiovascular

CG FUTURE ANNULOPLASTY SYSTEM, MODEL 638R

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

Ring, Annuloplasty

FDA classification

FDA Class 2 ·Ring, Annuloplasty

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)