McKesson Radiology Mammography Plus

FDA registration

CHANGE HEALTHCARE CANADA COMPANY·1 product·🇨🇦 Canada

McKesson Radiology Mammography Plus

FDA 510(k)

FDA Class 2 ·Radiology

Ophthalmic Scissors

FDA UDI

KATENA PRODUCTS, INC.·00841668105283·CASTROVIEJO SCISSORS ANGLED MEDIUM

TURNCO TOOL & INSTRUMENT, INC.

FDA registration

TURNCO TOOL & INSTRUMENT, INC.·1 product·🇺🇸 United States

Talos®-C

FDA registration

SPINEART SA·1 product·🇨🇭 Switzerland

Sterigenics Belgium Fleurus SA

FDA registration

Sterigenics Belgium Fleurus SA·1 product·🇧🇪 Belgium

Synergy Health Daniken AG

FDA registration

Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

Tutopatch DM Graft

FDA registration

Tutogen Medical GmBH·1 product·🇩🇪 Germany

Integra Bovine Pericardium Dural Graft

FDA registration

BBF STERILISATIONSSERVICE GMBH·1 product·🇩🇪 Germany

Machining Midtown LLC

FDA registration

Machining Midtown LLC·1 product·🇺🇸 United States

Tutopatch DM Graft

FDA registration

RTI Surgical, Inc. (dba RTI Biologics, Inc.)·1 product·🇺🇸 United States

AXIAL MEDICAL

FDA registration

AXIAL MEDICAL·1 product·🇺🇸 United States

Talos®-C

FDA registration

ALPES CN SAS·1 product·🇫🇷 France

Talos®-C

FDA registration

ALPES CN·1 product·🇫🇷 France

Talos®-C

FDA registration

Alpes CN·1 product·🇫🇷 France

TREESTONE TRADING GROUP LTD

FDA registration

TREESTONE TRADING GROUP LTD·1 product·🇺🇸 United States

TALOS-C CERVICAL INTERVERTEBRAL BODY FUSION DEVICES

FDA 510(k)

FDA Class 2 ·Orthopedic

CARDIODRIVE, MODEL 001-004115 (NON-STERILE); 001-1169-1 (STERILE)

FDA 510(k)

FDA Class 2 ·Cardiovascular

System, Image Processing, Radiological

FDA classification

FDA Class 2 ·System, Image Processing, Radiological

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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