Puregraft8291 (WP) - Puregraft 250 System

FDA registration

Synergy Health Westport Ltd·1 product·🇮🇪 Ireland

Solta Medical, Inc.

FDA registration

Solta Medical, Inc.·1 product·🇺🇸 United States

CYTORI PUREGRAFT 250/PURE SYSTEM

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

System, Suction, Lipoplasty

FDA classification

FDA Class 2 ·System, Suction, Lipoplasty

SYNTHES MATRIX SYSTEM; K092929

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·5 products·🇺🇸 United States

Dynamic Joint Distractor II

FDA registration

STRYKER GmbH·2 products·🇨🇭 Switzerland

INTERNATIONAL STERILIZATION LABORATORY, LLC

FDA registration

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

DJD II BODY

FDA registration

MAWATEC AG·2 products·🇨🇭 Switzerland

STERILIZATION SERVICES OF GEORGIA, INC.

FDA registration

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

EP-4™ Cardiac Stimulator, Cardiac Stimulator

FDA registration

St. Jude Medical, Cardiology Division, Inc.·1 product·🇺🇸 United States

Prolong

FDA registration

Avanos Medical, Inc. (Formerly Halyard Health Inc.)·1 product·🇺🇸 United States

EP-4™ Cardiac Stimulator, Cardiac Stimulator

FDA registration

St. Jude Medical, Atrial Fibrillation Division, Inc.·1 product·🇺🇸 United States

EP-4™ Cardiac Stimulator, Cardiac Stimulator

FDA registration

St. Jude Medical·1 product·🇺🇸 United States

DYNAMIC JOINT DISTRACTOR II EXTERNAL FIXATION SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

ARTHREX FIBERWIRE, USP SIZE 5, MODEL AR-7201

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

FDA classification

FDA Class 2 ·Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite

Suture, Nonabsorbable, Synthetic, Polyethylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polyethylene