OsteoFab Patient Specific Facial Device - Optimized

FDA registration

OXFORD PERFORMANCE MATERIALS, INC.·1 product·🇺🇸 United States

OsteoFab Patient Specific Facial Device

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

FDA classification

FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

DRE Waveline Pro Monitor

FDA registration

DRE Med·1 product·🇺🇸 United States

WUHAN STRONG ELECTRONICS

FDA registration

WUHAN STRONG ELECTRONICS·1 product·🇨🇳 China

IntelliVue MP20-MP90

FDA registration

Philips Electronics Ltd·1 product·🇨🇦 Canada

IntelliVue MP20-MP90

FDA registration

Philips Medizin Systeme Boeblingen GmbH·1 product·🇩🇪 Germany

Omni III

FDA registration

INFINIUM MEDICAL, INC.·1 product·🇺🇸 United States

GalaFLEX 3D

FDA registration

Tepha, Incorporated·1 product·🇺🇸 United States

GC Initial ZR Disk ML Elite

FDA registration

GC AMERICA INC.·1 product·🇺🇸 United States

Kyocera Medical Technologies, Inc.

FDA UDI

KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523104031·T³ Acetabular Hemispherical Shell, Cluster Hole...

THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90

FDA 510(k)

FDA Class 2 ·Cardiovascular

OMNI III PATIENT MONITOR

FDA 510(k)

FDA Class 2 ·Cardiovascular

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

FDA classification

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

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)