Modern Dental Laboratory (DG) Co., Ltd.

FDA registration

Modern Dental Laboratory (DG) Co., Ltd.·1 product·🇨🇳 China

Respire Blue EF+; Respire Pink EF Micro

FDA registration

DYNA FLEX·1 product·🇺🇸 United States

Blue Series EF

FDA registration

HEXA CERAM CO., LTD.·1 product·🇹🇭 Thailand

Modern Dental Global Solutions Limited

FDA registration

Modern Dental Global Solutions Limited·1 product·🇭🇰 Hong Kong

Modern Dental International Trading Limited

FDA registration

Modern Dental International Trading Limited·1 product·🇭🇰 Hong Kong

Respire Blue Series-EF

FDA 510(k)

FDA Class 2 ·Dental

HairCheck-DT (Cocaine)

FDA UDI

Quest Diagnostics·00868586000216·HairCheck-DT (Cocaine) is an ELISA test kit use...

KMEDIC

FDA UDI

TELEFLEX INCORPORATED·24026704284034·DEEP RAKE RETRACTOR 10 1/2" 1 1/2"

Device, Anti-Snoring

FDA classification

FDA Class 2 ·Device, Anti-Snoring

Reprocessed Electrophysiology Catheter

FDA registration

Stryker Sustainability Solutions·1 product·🇺🇸 United States

Reprocessed Electrophysiology Catheter

FDA registration

Stryker Sustainability Solutions Phoenix·1 product·🇺🇸 United States

catheter, recording, electrode reprocessed

FDA registration

Sterigenics US LLC·1 product·🇺🇸 United States

Spider Cervical Plating System - XSpine

FDA registration

NGInstruments, Inc dba Avalign Cutting Instruments·1 product·🇺🇸 United States

Spider Cervical Plating System

FDA registration

Xtant Medical Holdings, Inc.·1 product·🇺🇸 United States

StrykerSustainability6623 (SDA) - Reprocessed Electrode Recording Cable

FDA registration

Isomedix Operations Inc.·1 product·🇺🇸 United States

TBS iNsight

FDA registration

Medimaps Group SA·1 product·🇨🇭 Switzerland

REPROCESSED 2515 NAV VARIABLE ELECTROPHYSIOLOGY CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

SPIDER CERVICAL PLATING (SCP) SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Catheter, Recording, Electrode, Reprocessed

FDA classification

FDA Class 2 ·Catheter, Recording, Electrode, Reprocessed

Appliance, Fixation, Spinal Intervertebral Body

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body