SubFix

FDA registration

STRYKER GmbH·1 product·🇨🇭 Switzerland

SUBFIX ARTHROEREISIS IMPLANT, MODELS SUT0065, SUT0080, SUT0090, SUT0100, SUT0115

FDA 510(k)

FDA Class 2 ·Orthopedic

Microkeratome Blade

FDA registration

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

Finn Chambers

FDA registration

SMART PRACTICE·1 product·🇺🇸 United States

AngioAssist Family

FDA registration

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

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·2 products·🇨🇷 Costa Rica

VivoSight

FDA registration

MICHELSON DIAGNOSTICS LTD·1 product·🇬🇧 United Kingdom

Electrode, needle

FDA registration

CBR ENTERPRISE LIMITED·1 product·🇭🇰 Hong Kong

FINN CHAMBER (R)

FDA 510(k)

FDA Class 1 ·General Hospital

DISPOSABLE CB-PE MICROKERATOME BLADES

FDA 510(k)

FDA Class 1 ·Ophthalmic

Applicator, Absorbent Tipped, Non-Sterile

FDA classification

FDA Class 1 ·Applicator, Absorbent Tipped, Non-Sterile

Screw, Fixation, Bone

FDA classification

FDA Class 2 ·Screw, Fixation, Bone

Keratome, Ac-Powered

FDA classification

FDA Class 1 ·Keratome, Ac-Powered