OMNIPORE(R) Surgical Implant

FDA registration

MATRIX SURGICAL HOLDINGS, LLC dba MATRIX SURGICAL USA·1 product·🇺🇸 United States

OMNIPORE SURGICAL IMPLANTS AND ACCESSORIES

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

FDA classification

FDA Class 2 ·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction

Leukomed®

FDA UDI

BSN medical GmbH·04042809802979·LEUKOMED SKIN SENSITIVE STERILE 5X7.2CM WHITE 10

Nipro (Thailand) Corporation Limited

FDA registration

Nipro (Thailand) Corporation Limited·1 product·🇹🇭 Thailand

HydroFill Filar Modification

FDA registration

MicroVention, Inc.·2 products·🇺🇸 United States

Vacuette Safety Blood Collection / Infusion Set

FDA registration

GREINER BIO-ONE GMBH·1 product·🇦🇹 Austria

CBR ENTERPRISE LIMITED

FDA registration

CBR ENTERPRISE LIMITED·1 product·🇭🇰 Hong Kong

NIPRO CORPORATION

FDA registration

NIPRO CORPORATION·1 product·🇯🇵 Japan

InfraredX

FDA registration

MICROTEK DOMINICANA, S.A.·3 products·🇩🇴 Dominican Republic

Imaging System

FDA registration

Sterigenics U.S., LLC·3 products·🇺🇸 United States

Lyra Direct C.difficile Assay

FDA registration

Ortho-Clinical Diagnostics, Inc.·2 products·🇺🇸 United States

INTERPORE CROSS CEMENT RESTRICTOR

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

HYDROCOIL EMBOLIC SYSTEM (HES)

FDA 510(k)

FDA Class 2 ·Neurology

Prosthesis, Hip, Cement Restrictor

FDA classification

FDA Class 2 ·Prosthesis, Hip, Cement Restrictor

Device, Neurovascular Embolization

FDA classification

FDA Class 2 ·Device, Neurovascular Embolization