TRACHEOBRONXANE™ DUMON®

FDA registration

NOVATECH S.A.·1 product·🇫🇷 France

TRACHEOBRONXANE™ DUMON®

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Prosthesis, Tracheal, Preformed/Molded

FDA classification

FDA Class 2 ·Prosthesis, Tracheal, Preformed/Molded

Ophthalmic Cannula

FDA UDI

KATENA PRODUCTS, INC.·00841668113912·VISCO INJECTION CANNULA 23GA

Renovis S141 Lumbar Interbody Cage System

FDA registration

Kyocera Medical Technologies, Inc.·1 product·🇺🇸 United States

PLIF

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

PLIF

FDA registration

Sterigenics US, LLC·1 product·🇺🇸 United States

ASSIST HEADER CLEANER

FDA registration

MOLDED PRODUCTS INC.·1 product·🇺🇸 United States

PLIF

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

PERI-LOC PERIARTICULAR AND VARIABLE- ANGLE LOCKED PLATING (VLP) SYSTEMS

FDA registration

Smith & Nephew, Inc.·7 products·🇺🇸 United States

PERI-LOC PERIARTICULAR AND VARIABLE- ANGLE LOCKED PLATING (VLP) SYSTEMS

FDA registration

Smith & Nephew, Inc.·7 products·🇺🇸 United States

Renovis S141 Lumbar Interbody Cage System

FDA 510(k)

FDA Class 2 ·Orthopedic

ASSIST HEADER CLEANER

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

Dialyzer Reprocessing System

FDA classification

FDA Class 2 ·Dialyzer Reprocessing System

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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