AR-7234

FDA registration

BRDH·1 product·🇳🇱 Netherlands

Arthrex New Zealand Limited

FDA registration

Arthrex New Zealand Limited·1 product·🇳🇿 New Zealand

BIOGENOMICS S.A.C. - BIOCELLS SURGICAL

FDA registration

BIOGENOMICS S.A.C. - BIOCELLS SURGICAL·1 product·🇵🇪 Peru

Arthrex Australia Pty Ltd.

FDA registration

Arthrex Australia Pty Ltd.·1 product·🇦🇺 Australia

I-MEDICAL ASIA COMPANY LIMITED

FDA registration

I-MEDICAL ASIA COMPANY LIMITED·1 product·🇭🇰 Hong Kong

ARTHREX, INC.

FDA registration

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

Arthrex, Inc.

FDA registration

Arthrex, Inc.·1 product·🇺🇸 United States

Arthrex Manufacturing Inc.

FDA registration

Arthrex Manufacturing Inc.·1 product·🇺🇸 United States

Arthrex LoopLoc Knotless Suture

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Suture, Nonabsorbable, Synthetic, Polyethylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polyethylene

Dornier MedTech

FDA UDI

Dornier MedTech GmbH·04049958001925·600 Micron Disposable Diode Laser Lightguide, 6...

Dornier MedTech

FDA UDI

DORNIER MEDTECH AMERICA, INC.·00810116022601·Dornier 600 µm Single-Use SMA UroBeam Diode Las...

Cannulated Compression Device System

FDA registration

Orthopedic Designs North America, Inc.·1 product·🇺🇸 United States

Model 96102

FDA registration

Spacelabs Healthcare Inc.·4 products·🇺🇸 United States

Relivion

FDA registration

NEUROLIEF Inc.·1 product·🇺🇸 United States

XHIBIT CENTRAL STATION, MODEL 96102

FDA 510(k)

FDA Class 2 ·Cardiovascular

Cannulated Compression Device System

FDA 510(k)

FDA Class 2 ·Orthopedic

Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)

Screw, Fixation, Bone

FDA classification

FDA Class 2 ·Screw, Fixation, Bone