InterFuse S Intervertebral Body Fusion Device

FDA registration

NEXT ORTHOSURGICAL·1 product·🇺🇸 United States

INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE

FDA 510(k)

FDA Class 2 ·Orthopedic

K080633

FDA registration

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

Actera hip system

FDA UDI

Conformis, Inc.·00810933031404·Actera Stem Digital Template

RICHARD WOLF GMBH

FDA registration

RICHARD WOLF GMBH·1 product·🇩🇪 Germany

INTERNATIONAL STERILIZATION LABORATORY, LLC

FDA registration

INTERNATIONAL STERILIZATION LABORATORY, LLC·1 product·🇺🇸 United States

STERILIZATION SERVICES OF GEORGIA, INC.

FDA registration

STERILIZATION SERVICES OF GEORGIA, INC.·1 product·🇺🇸 United States

Arthrex, Inc.

FDA registration

R.K. Manufacturing·1 product·🇺🇸 United States

Isomedix Operations Inc.

FDA registration

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

ARTHREX FIBERWIRE, MODEL SPU-02NB-3800

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

HYSTEROSCOPE OPERATING SHEATH AND INSERT, MODEL 8988.031/.041/.231/.241

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Hysteroscope (And Accessories)

FDA classification

FDA Class 2 ·Hysteroscope (And Accessories)

Suture, Nonabsorbable, Synthetic, Polyethylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polyethylene