FORZA Ti Spacer System

FDA registration

ORTHOFIX US LLC·1 product·🇺🇸 United States

FORZA Ti Spacer System

FDA 510(k)

FDA Class 2 ·Orthopedic

RONGXING PLASTIC JURONG CO.,LTD.

FDA registration

RONGXING PLASTIC JURONG CO.,LTD.·1 product·🇨🇳 China

MIM 5.2 (Brachy)

FDA registration

ELEKTA SOLUTIONS AB·1 product·🇸🇪 Sweden

MIM Symphony Bx

FDA registration

MIM SOFTWARE INC.·1 product·🇺🇸 United States

Ophthalmic Cannula

FDA UDI

KATENA PRODUCTS, INC.·00841668114278·CHAMBER MAINTAINER 20GA (PK/10)

Oph. Cystotomes

FDA UDI

KATENA PRODUCTS, INC.·00841668113745·CCC CYSTOTOME FORMED 27GA

Ophthalmic Cannula

FDA UDI

KATENA PRODUCTS, INC.·00841668114063·MCINTYRE-BINKHORST CAN 25GA ANG RT PK/10

Boston Scientific Corp., Marina Bay Cust. Fulfillment Center

FDA registration

Boston Scientific Corp., Marina Bay Cust. Fulfillment Center·4 products·🇺🇸 United States

Perla TL MIS

FDA registration

SPINEART SA·2 products·🇨🇭 Switzerland

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·4 products·🇺🇸 United States

LENS Connected Tower Application, 72205347

FDA registration

SMITH & NEPHEW INC.·1 product·🇺🇸 United States

Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503

FDA 510(k)

FDA Class 2 ·Cardiovascular

MIM 5.2 (BRACHY)

FDA 510(k)

FDA Class 2 ·Radiology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Detector And Alarm, Arrhythmia

FDA classification

FDA Class 2 ·Detector And Alarm, Arrhythmia

System, Image Processing, Radiological

FDA classification

FDA Class 2 ·System, Image Processing, Radiological