Set PP

FDA registration

SDI LTD.·1 product·🇦🇺 Australia

SET PP

FDA 510(k)

FDA Class 2 ·Dental

K073033

FDA registration

IMPLANT DIRECT SYBRON MANUFACTURING LLC·1 product·🇺🇸 United States

Surgical Titanium Mesh

FDA registration

Synthes GMBH·1 product·🇨🇭 Switzerland

Paragon Medical Inc.

FDA registration

Paragon Medical Inc.·1 product·🇺🇸 United States

Surgical Titanium Mesh

FDA registration

DEPUY SPINE, INC.·1 product·🇺🇸 United States

HL168N

FDA registration

LIVING SCIENCE CO., LTD.·1 product·🇨🇳 China

TOMZ Corporation

FDA registration

TOMZ Corporation·1 product·🇺🇸 United States

HL168N

FDA registration

HEALTH & LIFE MEDICAL TECHNOLOGY COMPANY LIMITED·1 product·🇻🇳 Vietnam

HL168N

FDA registration

Health & Life Corporation·1 product·🇹🇼 Taiwan

Surgical Titanium Mesh

FDA registration

Jabil Switzerland Manufacturing GmbH (Le Locle)·1 product·🇨🇭 Switzerland

Citizen Systems Japan CH607

FDA registration

CITIZEN SYSTEMS JAPAN CO., LTD.·1 product·🇯🇵 Japan

Surgical Titanium Mesh

FDA registration

SYNTHES GMBH·1 product·🇨🇭 Switzerland

Titanium Screws

FDA registration

DEPUY ORTHOPAEDICS·1 product·🇺🇸 United States

Surgical Mesh

FDA registration

BIEDERMANN MOTECH GMBH & Co. KG·1 product·🇩🇪 Germany

Colposcope

FDA registration

BEIJING TECH INSTRUMENT CO., LTD.·1 product·🇨🇳 China

CANDELA CLEARBEAM PULSED DYE LASER

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

SURGICAL TITANIUM MESH SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Cement, Dental

FDA classification

FDA Class 2 ·Cement, Dental

Spinal Vertebral Body Replacement Device

FDA classification

FDA Class 2 ·Spinal Vertebral Body Replacement Device