DIOSLIMON IMPLANT SYSTEM

FDA registration

DIO Corporation·1 product·🇰🇷 South Korea

DIOSLIMON IMPLANT SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

5550 1/2L SYRINGE

FDA UDI

HANS RUDOLPH, INC.·00874750009961·5550D 1/2L SYR 1.125/22MM OUTL

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776305109·COLLIER-ANDERSON CLAMP CVD 11"

RESMED CORP

FDA registration

RESMED CORP·1 product·🇺🇸 United States

RMO

FDA registration

RMO·1 product·🇲🇾 Malaysia

ResMed Asia Pte. Ltd.

FDA registration

ResMed Asia Pte. Ltd.·1 product·🇸🇬 Singapore

TomTec Radiology Ultrasound Standard

FDA registration

CANON MEDICAL INFORMATICS, INC.·2 products·🇺🇸 United States

RESMED PTY LTD.

FDA registration

RESMED PTY LTD.·1 product·🇦🇺 Australia

VIV for Your V

FDA registration

BRISAR INDUSTRIES INC·1 product·🇺🇸 United States

MIRAGE FX

FDA 510(k)

FDA Class 2 ·Anesthesiology

ICE BATON

FDA 510(k)

FDA Unclassified ·Unknown

Device, Thermal, Hemorrhoids

FDA classification

FDA Unclassified ·Device, Thermal, Hemorrhoids

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form

Ventilator, Non-Continuous (Respirator)

FDA classification

FDA Class 2 ·Ventilator, Non-Continuous (Respirator)