BluePrint

FDA registration

Tornier S.A.S.·1 product·🇫🇷 France

BluePrint

FDA registration

IMASCAP·1 product·🇫🇷 France

BLUEPRINT Patient Specific Instrumentation

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

FDA classification

FDA Class 2 ·Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Catheter

FDA registration

Nypro Inc (Maple Grove)·1 product·🇺🇸 United States

Isomedix Operations, Inc.

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

XLP Lateral Plate System

FDA registration

NUVASIVE, INC.·1 product·🇺🇸 United States

XLP Lateral Plate System

FDA registration

NUVASIVE, INC.·1 product·🇺🇸 United States

XLP Lateral Plate

FDA registration

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

Reprocessed EP Catheters

FDA registration

STERILMED, INC.·1 product·🇺🇸 United States

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·1 product·🇺🇸 United States

Shang Ring

FDA registration

Wuhu Snnda Medical Treatment Appliance Technology Co. Ltd.·1 product·🇨🇳 China

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·1 product·🇨🇷 Costa Rica

Sterigenics US LLC

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

LATERAL PLATE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

REPROCESSED ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Recording, Electrode, Reprocessed

FDA classification

FDA Class 2 ·Catheter, Recording, Electrode, Reprocessed

Appliance, Fixation, Spinal Intervertebral Body

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body