KMTI S141 Lumbar Interbody Fusion System

FDA registration

Kyocera Medical Technologies, Inc.·1 product·🇺🇸 United States

KMTI S141 Lumbar Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

MaXcess

FDA UDI

Nuvasive, Inc.·00887517187444·MaXcess Access Blade, 70mm Right

NuVasive

FDA UDI

Nuvasive, Inc.·00195377105141·NTS Slot Tube, 20x70mm Beveled

Medical Endoscope Image Processing System

FDA registration

JIANGSU JIYUAN MEDICAL TECHNOLOGY CO., LTD.·1 product·🇨🇳 China

Medley Hybrid Lubricant

FDA registration

GOOD CLEAN LOVE, INC.·1 product·🇺🇸 United States

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776189150·HANDLE FOR ESOPHAGOSCOPE

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112564·BARRON CORNEAL PUNCH 6.0MM

NA

FDA UDI

Stryker Leibinger GmbH & Co. KG·07613153168478·BIPOLAR FORCEPS

Ti-Fix OLIF Spacer

FDA UDI

Tyber Medical LLC·M695P32120700·Ti-Fix OLIF Spacer 32 x 12 x 7 (mm) x 0 °

HONOUR™ Spacer System

FDA UDI

NEXXT SPINE, LLC·00889929002810·Cervical PEEK, 6°, 12mm W x 12mm D x 7mm H

Duray Imaging Plate Scanner, Model:DC1

FDA registration

BEYES DENTAL INC·1 product·🇨🇦 Canada

HONOUR™ Spacer System

FDA UDI

NEXXT SPINE, LLC·00889929002827·Cervical PEEK, 0°, 12mm W x 12mm D x 7mm H

ORALLITE COMPREHENSIVE EXAM TRAY

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.014 GUIDE WIRE, CHOCOLATE PTA BALLOON CATHETER (OVER THE WIRE) 0.18 G

FDA 510(k)

FDA Class 2 ·Cardiovascular

Source, Chemiluminescent Light

FDA classification

FDA Class 2 ·Source, Chemiluminescent Light

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Catheter, Angioplasty, Peripheral, Transluminal

FDA classification

FDA Class 2 ·Catheter, Angioplasty, Peripheral, Transluminal