Biomesh® P1 and Biomesh® Plug and Patch

FDA registration

Sterigenics SAS·1 product·🇫🇷 France

BIOMESH P1 AND BIOMESH PLUG AND PATCH

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Henry Schein

FDA UDI

HENRY SCHEIN, INC.·00304040044674·Akers Spoon Only

Custom Procedure Kit

FDA UDI

MEDIVATORS INC.·40677964018822·Endo Carry-On Procedure Kit

GC Fuji Filling™

FDA UDI

Gc America Inc.·D0470024791·GC Fuji Filling™ CV, 8 g (3.9 mL) cartridge, mi...

GC Fuji Filling™

FDA UDI

Gc America Inc.·14548161394314·GC Fuji Filling™ CV, 8 g (3.9 mL) cartridge, mi...

Instrument Wipe ML115

FDA registration

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

ML110 CleanTouch PVA Eye Spear

FDA registration

MED-LOGICS, INC.·1 product·🇺🇸 United States

MAGNETOM ALLEGRA SYSTEM

FDA registration

Siemens Healthineers AG·1 product·🇩🇪 Germany

Instrument Wipe ML115

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

CONTROLLER, FOOT, HANDPIECE AND CORD

FDA registration

Millstone Medical Outsourcing LLC·1 product·🇺🇸 United States

VITROS Calibrator Kit 13

FDA registration

ORTHO-CLINICAL DIAGNOSTICS, INC.·3 products·🇺🇸 United States

VITROS Calibrator Kit 13

FDA registration

ORTHO-CLINICAL DIAGNOSTICS, INC.·3 products·🇺🇸 United States

VITROS Calibrator Kit 13

FDA registration

Ortho-Clinical Diagnostics European Support Center·3 products·🇫🇷 France

PALCERAM 53

FDA 510(k)

FDA Class 2 ·Dental

MULTI-FUNCTION DEFIBRILLATION ELECTRODE

FDA 510(k)

FDA Class 3 ·Cardiovascular

Mesh, Surgical, Polymeric

FDA classification

FDA Class 2 ·Mesh, Surgical, Polymeric

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)

Alloy, Gold-Based Noble Metal

FDA classification

FDA Class 2 ·Alloy, Gold-Based Noble Metal