Self Drilling Screw

FDA registration

BIOMET MICROFIXATION·1 product·🇺🇸 United States

LORENZ SELF DRILLING SCREWS

FDA registration

Changzhou Biomet Medical Devices Co., Ltd.·1 product·🇨🇳 China

LORENZ SELF DRILLING SCREWS

FDA registration

BIOMET, INC.·1 product·🇺🇸 United States

LORENZ SELF DRILLING SCREWS

FDA 510(k)

FDA Class 2 ·Orthopedic

GlobalCardio

FDA registration

CARDIOCOMM SOLUTIONS, INC.·1 product·🇨🇦 Canada

Catheter, Percutaneous

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450675106·

BETSEY JOHNSON

FDA UDI

FGX INTERNATIONAL INC.·00193033544990·

BETSEY JOHNSON

FDA UDI

FGX INTERNATIONAL INC.·00193033545010·

BETSEY JOHNSON

FDA UDI

FGX INTERNATIONAL INC.·00193033545003·

BETSEY JOHNSON

FDA UDI

FGX INTERNATIONAL INC.·00193033544983·

DIVERSATEK HEALTHCARE INC.

FDA registration

DIVERSATEK HEALTHCARE INC.·1 product·🇺🇸 United States

Diversatek Vietnam Company Limited

FDA registration

Diversatek Vietnam Company Limited·1 product·🇻🇳 Vietnam

BIOFIRE SPOTFIRE Module

FDA registration

BioFire Diagnostics, LLC·10 products·🇺🇸 United States

STIMULAN - CALCIUM SULFATE BONE VOID FILLER KIT

FDA 510(k)

FDA Class 2 ·Orthopedic

CONCENTRIC BALLOON GUIDE CATHETER, MODEL 90031

FDA 510(k)

FDA Class 2 ·Cardiovascular

Screw, Fixation, Bone

FDA classification

FDA Class 2 ·Screw, Fixation, Bone

Filler, Bone Void, Calcium Compound

FDA classification

FDA Class 2 ·Filler, Bone Void, Calcium Compound

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous