AMII Implant System

FDA registration

INNOBIOSURG CO., LTD.·2 products·🇰🇷 South Korea

Magicore Narrow System

FDA 510(k)

FDA Class 2 ·Dental

X-CORE

FDA UDI

Nuvasive, Inc.·00887517434296·X-CORE 2 Ti Core, Ø22x47-79mm

ClearPoint System and Accessories

FDA registration

ClearPoint Neuro Inc.·1 product·🇺🇸 United States

SMARTFrame Accessory Kit (7F)

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

ML7061 Calibrated LASIK Blade (CLB)

FDA registration

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

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112649·BARRON CORNEAL PUNCH 8.25MM

BLADEWORKS MICROKERATOME BLADE, MODEL 7061

FDA 510(k)

FDA Class 1 ·Ophthalmic

PRIMED TRACHEOSTOMY TUBES (MULTIPLE)

FDA 510(k)

FDA Class 2 ·Anesthesiology

NA

FDA UDI

Zimmer, Inc.·00889024187870·

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form

Keratome, Ac-Powered

FDA classification

FDA Class 1 ·Keratome, Ac-Powered

Tube, Tracheostomy (W/Wo Connector)

FDA classification

FDA Class 2 ·Tube, Tracheostomy (W/Wo Connector)