Spine Smith 0601-0090 Cynch TLIF: 5° x 11mm x 30mm x 9mm

FDA registration

BANISTER TOOL, INC.·1 product·🇺🇸 United States

Intervertebral fusion device with bone graft, lumbar

FDA registration

SpineSmith Holdings, LLC·1 product·🇺🇸 United States

SPINESMITH CYNCH SPINAL SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Electronic Light Guide

FDA registration

CONMED CORPORATION·1 product·🇺🇸 United States

Electronic Light Guide

FDA registration

Consolidated Medical Equipment Company·1 product·🇲🇽 Mexico

Glass Ionomer Aesthetic Restorative

FDA registration

ADVANCED HEALTHCARE LTD.·2 products·🇬🇧 United Kingdom

Electronic Light Guide

FDA registration

Linvatec Corporation d/b/a ConMed Linvatec·1 product·🇺🇸 United States

N/A

FDA UDI

BIOMET MICROFIXATION, INC·00841036029050·

Merit Medical®

FDA UDI

Merit Medical Systems, Inc.·00884450047750·

RMS CO.

FDA registration

RMS CO.·1 product·🇺🇸 United States

FMI-Silicone Urinary Catheter

FDA registration

FOOTPRINT MEDICAL INC.·1 product·🇺🇸 United States

AHL GENERIC GLASS IONOMER AESTHETIC RESTORATIVE

FDA 510(k)

FDA Class 2 ·Dental

SPECIALTY 42 (HEFILCON A) HYDROPHILIC CONTACT LENS FOR DAILY WEAR, SPECIALTY T-42 TORIC (HEFILCON A) HYDROPHILIC CONTACT

FDA 510(k)

FDA Class 2 ·Ophthalmic

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Cement, Dental

FDA classification

FDA Class 2 ·Cement, Dental

Lenses, Soft Contact, Daily Wear

FDA classification

FDA Class 2 ·Lenses, Soft Contact, Daily Wear