iQ Flex Pro

FDA registration

FIRST SOURCE INC.·1 product·🇺🇸 United States

iQFlex Pro

FDA 510(k)

FDA Class 2 ·Radiology

MaXcess

FDA UDI

Nuvasive, Inc.·00887517431905·MaXcess 4 Inserter, Low Profile Shim

Freelite® Human Lambda Free kit For use on the Roche cobas® c systems

FDA registration

The Binding Site Group Ltd.·2 products·🇬🇧 United Kingdom

Freelite® Human Lambda Free kit For use on the Roche cobas® c systems

FDA registration

THE BINDING SITE·2 products·🇬🇧 United Kingdom

Soprano ICE

FDA registration

ALMA LASERS LTD.·2 products·🇮🇱 Israel

System, X-Ray, Mobile

FDA classification

FDA Class 2 ·System, X-Ray, Mobile

NA

FDA UDI

SYNTHES (U.S.A.) LP·10886982164261·4.5MM PROXIMAL TIBIA PLATE 8 HOLES/LEFT

Stent, Carotid

FDA Pre-Market Approval

FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection

Plateau-X Spacer System

FDA UDI

Life Spine, Inc.·00190837012458·

M/DN®

FDA UDI

Zimmer, Inc.·00889024040076·

M/DN®

FDA UDI

Zimmer, Inc.·00889024040090·

M/DN®

FDA UDI

Zimmer, Inc.·00889024040083·

Bipolar Head Fitting Screw

FDA UDI

SIGNATURE ORTHOPAEDICS PTY LTD·09348215098858·

Zio AT device

FDA registration

iRhythm Technologies, Inc.·4 products·🇺🇸 United States

EZ Bond Universal

FDA registration

META BIOMED CO., LTD.·1 product·🇰🇷 South Korea

clonoSEQ® Assay

FDA registration

ADAPTIVE BIOTECHNOLOGIES·1 product·🇺🇸 United States

clonoSEQ® Assay

FDA registration

ADAPTIVE BIOTECHNOLOGIES·1 product·🇺🇸 United States

Spud

FDA UDI

KATENA PRODUCTS, INC.·00841668101209·GOLF CLUB FOREIGN BODY SPUD

FREELITE HUMAN KAPPA AND LAMBDA KITS

FDA 510(k)

FDA Class 2 ·Immunology