MLX - Medial Lateral Expandable Lumbar Interbody

FDA registration

NUVASIVE, INC.·1 product·🇺🇸 United States

MLX

FDA registration

GLOBUS MEDICAL, INC.·1 product·🇺🇸 United States

MLX - MEDIAL LATERAL EXPANDABLE LUMBAR INTERBODY SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

GYRUS ACMI, INC

FDA UDI

Gyrus Acmi, Inc.·00821925016224·PLS PIST W/ARM-STYLE LP

MILLSTONE MEDICAL OUTSOURCING LLC.

FDA registration

MILLSTONE MEDICAL OUTSOURCING LLC.·1 product·🇺🇸 United States

Vanguard Patella Components

FDA registration

SYMMETRY MEDICAL MANUFACTURING INC·1 product·🇺🇸 United States

PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

FDA registration

Zimmer Biomet Centroamerica SA·1 product·🇨🇷 Costa Rica

Vanguard Patella Components

FDA registration

SYMMETRY MEDICAL MANUFACTURING INC.·1 product·🇺🇸 United States

Microcutter Xchange

FDA registration

Sterigenics U.S. LLC·1 product·🇺🇸 United States

ZIMMER PTE. LTD.

FDA registration

ZIMMER PTE. LTD.·1 product·🇸🇬 Singapore

Zimmer Biomet Pty Ltd

FDA registration

Zimmer Biomet Pty Ltd·1 product·🇦🇺 Australia

Zimmer (Shanghai) Medical International Trading Co., Ltd.

FDA registration

Zimmer (Shanghai) Medical International Trading Co., Ltd.·1 product·🇨🇳 China

VANGUARD PATELLA COMPONENTS

FDA registration

BIOMET, INC.·1 product·🇺🇸 United States

Zimmer (LN) - VANGUARD PATELLA COMPONENTS

FDA registration

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

Suzhou Armocon Technology Co., Ltd.

FDA registration

Suzhou Armocon Technology Co., Ltd.·1 product·🇨🇳 China

SHILLA™ Growth Guidance System

FDA registration

C&A Tool Engineering, Inc. Auburn Plant·1 product·🇺🇸 United States

LELO USA INC.

FDA registration

LELO USA INC.·1 product·🇺🇸 United States

VANGUARD PATELLA COMPONENTS

FDA 510(k)

FDA Class 2 ·Orthopedic

HEALTHTRACKER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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