LnK Lumbar Interbody Fusion Cage System

FDA registration

L&K BIOMED CO.,LTD.·1 product·🇰🇷 South Korea

LnK Lumbar Interbody Fusion Cage System

FDA 510(k)

FDA Class 2 ·Orthopedic

RUSCH

FDA UDI

TELEFLEX INCORPORATED·14026704630858·Rusch Polaris FO Blade, Mac 4, Sterile

AGC TRADITION KNEE SYSTEM

FDA UDI

Biomet Orthopedics, LLC·00880304241251·

Globe Scientific

FDA UDI

GLOBE SCIENTIFIC INC.·00840095620215·Pipette tip, 1-200uL, natural for MLA

BLT Profile Drill, long

FDA UDI

BIO CONCEPT CO.,LTD·06947600304142·

FUSION-DOE

FDA registration

DENTLIGHT INC.·2 products·🇺🇸 United States

PROLTYE® Electrolyte Analyzer

FDA registration

Diamond Diagnostics Inc.·4 products·🇭🇺 Hungary

PROLTYE® Electrolyte Analyzer

FDA registration

DIAMOND DIAGNOSTICS Inc·4 products·🇺🇸 United States

APEX Knee System

FDA UDI

Omni Life Science, Inc.·00841690192404·Apex Revision Knee Reamer - Zimmer 14mm

IPB Inc

FDA registration

IPB Inc·1 product·🇺🇸 United States

STARband, STARlight

FDA registration

ORTHOMERICA PRODUCTS, INC.·2 products·🇺🇸 United States

OsteoMed

FDA UDI

OSTEOMED LLC·00845694046794·PrimaLIF LLIF PEEK Implant, 11mm X 18mm X 40mm,...

DENTLIGHT ORAL EXAM LIGHT KIT

FDA 510(k)

FDA Class 2 ·Dental

PROLYTE ELECTROLYTE ANALYZER

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

NA

FDA UDI

GENDRON, INC.·00842307103042·STRETCHER,CHR FRM,ENAM LTR

Diagnostic Light, Soft Tissue Detector

FDA classification

FDA Class 2 ·Diagnostic Light, Soft Tissue Detector

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Electrode, Ion Specific, Sodium

FDA classification

FDA Class 2 ·Electrode, Ion Specific, Sodium