CMI implant IS System

FDA registration

NEOBIOTECH CO., LTD.·1 product·🇰🇷 South Korea

SQ IS SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

CoRoent

FDA UDI

Nuvasive, Inc.·00887517297280·CoRoent® LO Ti, 8x10x25mm 10°

L-Dex U400

FDA registration

Impedimed Limited·1 product·🇦🇺 Australia

SR Applicator

FDA registration

USR ELECTRONIC SYSTEMS (1987) LTD·1 product·🇮🇱 Israel

AngioAssist Family

FDA registration

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

EPG Cover

FDA registration

Medtronic, Inc.·1 product·🇺🇸 United States

Electrode, needle

FDA registration

CBR ENTERPRISE LIMITED·1 product·🇭🇰 Hong Kong

EndoSync A.I.

FDA registration

J. MORITA MFG. CORP.·1 product·🇯🇵 Japan

MEDLINE STERISET STERILIZATION CONTAINER

FDA 510(k)

FDA Class 2 ·General Hospital

4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form

Wrap, Sterilization

FDA classification

FDA Class 2 ·Wrap, Sterilization

Catheter, Intravascular, Diagnostic

FDA classification

FDA Class 2 ·Catheter, Intravascular, Diagnostic