AVS PL PEEK Spacers

FDA registration

STRYKER SPINE·1 product·🇫🇷 France

AVS PL PEEK Spacers

FDA registration

STRYKER SPINE·1 product·🇺🇸 United States

AVS PL PEEK SPACERS, MODELS 48351XXX AND 48353XXX

FDA 510(k)

FDA Class 2 ·Orthopedic

ePTFE Sheet

FDA registration

IMPLANTECH ASSOCIATES, INC.·1 product·🇺🇸 United States

Tuttnauer Steam Sterilizer

FDA registration

TUTTNAUER LTD.·1 product·🇮🇱 Israel

EPTFE SHEETING

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING

FDA registration

EDWARDS LIFESCIENCES LLC·1 product·🇺🇸 United States

CARPENTIER-EDWARDS PHYSIO II ANNULOPLASTY RING

FDA registration

Edwards Lifesciences·1 product·🇨🇷 Costa Rica

MODIFICATION TO M2376A DEVICELINK SYSTEM

FDA 510(k)

FDA Class 2 ·Cardiovascular

EHS SERIES TABLE TOP AUTOCLAVE, MODELS 2540 AND 3870

FDA 510(k)

FDA Class 2 ·General Hospital

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Sterilizer, Steam

FDA classification

FDA Class 2 ·Sterilizer, Steam

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

FDA classification

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