LOSPA

FDA registration

CORENTEC CO., LTD.·1 product·🇰🇷 South Korea

LOSPA IS TLIF & DLIF Cages

FDA 510(k)

FDA Class 2 ·Orthopedic

ACS

FDA UDI

AMERICAN CONTRACT SYSTEMS, INC.·00191072016171·OPEN HEART DRAPE ACC PACK - 170243

Sutralene Polypropylene Sutures

FDA registration

AUROLAB·1 product·🇮🇳 India

SUTRALENE

FDA registration

VISIONARY MEDICAL SUPPLIES, INC.·1 product·🇺🇸 United States

AESCULAP AG

FDA registration

AESCULAP AG·1 product·🇩🇪 Germany

Aesculap, SC444R - Quintex All-in-one DBL GD SLV - Drill Guide

FDA registration

Complexus Medical·1 product·🇺🇸 United States

Lacriflow CL

FDA registration

KANEKA MEDIX CORPORATION KANAGAWA PLANT·1 product·🇯🇵 Japan

SupraSDRM

FDA registration

POLYMEDICS INNOVATIONS·1 product·🇩🇪 Germany

Suprathel

FDA registration

BBF STERILISATIONSSERVICE GMBH·1 product·🇩🇪 Germany

Lacriflow CL

FDA registration

Kaneka Corporation Osaka Plant·1 product·🇯🇵 Japan

Xiros8315 (DV) - Infinity-Lock Button System

FDA registration

SYNERGY HEALTH STERILISATION UK LTD·1 product·🇬🇧 United Kingdom

QUINTEX CERVICAL PLATING SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

SUTRALENE POLYPROPYLENE SUTURES

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Suture, Nonabsorbable, Synthetic, Polypropylene

FDA classification

FDA Class 2 ·Suture, Nonabsorbable, Synthetic, Polypropylene

Appliance, Fixation, Spinal Intervertebral Body

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body