L-Box®

FDA UDI

Innovasis, Inc.·M711XLC5010120·PEEK, Ti 6Al 4V (ELI)

L-Box®

FDA UDI

Innovasis, Inc.·M711XLB5508070·PEEK, Ti 6Al 4V (ELI)

Aqualizer Mouthpiece

FDA registration

JUMAR CORP.·1 product·🇺🇸 United States

THE OPTIC BOX CONTACT LENS CASE

FDA 510(k)

FDA Class 2 ·Ophthalmic

Intraocular Lens

FDA Pre-Market Approval

FDA Class 3 ·AMO SILICONE MONOFOCAL AND MULTIFOCAL INTRAOCULAR LENS

Ventilator, High Frequency

FDA Pre-Market Approval

FDA Class 3 ·LIFE PULSE HIGH FREQUENCY VENTILATOR

Lens, Multifocal Intraocular

FDA Pre-Market Approval

FDA Class 3 ·AMO SILICONE MONOFOCAL AND MULTIFOCAL INTRAOCULAR LENS

OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03

FDA 510(k)

FDA Class 2 ·Anesthesiology

Z-Robot

FDA registration

CHINAN BIOMEDICAL TECHNOLOGY, INC.·1 product·🇹🇼 Taiwan

Proton-LINAC 7

FDA registration

CHINAN BIOMEDICAL TECHNOLOGY, INC.·1 product·🇹🇼 Taiwan

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION

Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes

FDA Pre-Market Approval

FDA Class 3 ·CapSure Fix Novus Lead (4076, 5076)

Permanent Pacemaker Electrode

FDA Pre-Market Approval

FDA Class 3 ·MODEL 5076 CAPSURE FIX NOVUS ELECTRODE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval

FDA Class 2 ·INTER FIX TM THREADED FUSION DEVICE

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval

FDA Class 3 ·Maestro™ Ablation Connection Box, IntellaNav™ OI

FDA Pre-Market Approval

INTER FIX RP THREADED FUSION DEVICE

FDA Pre-Market Approval

INTER FIX RP THREADED FUSION DEVICE

FDA Pre-Market Approval

INTER FIX III THREADED FUSION DEVICE

PMMA BLOCK

FDA UDI

Huge Dental Material Co., Ltd.·06970402661434·

PMMA BLOCK

FDA UDI

Huge Dental Material Co., Ltd.·06970402661373·