MP LeFort I Plates

FDA registration

STRYKER LEIBINGER GMBH & CO. KG·1 product·🇩🇪 Germany

MP LeFort I Plates

FDA 510(k)

FDA Class 2 ·Dental

SR PIP

FDA UDI

Stryker Trauma SA·00886385020105·Trial Extractor, SR PIP

MAITLAND ENGINEERING

FDA registration

MAITLAND ENGINEERING·1 product·🇺🇸 United States

Electrodes

FDA registration

Cosmed Group Inc.·1 product·🇺🇸 United States

Highridge Medical, LLC

FDA registration

Highridge Medical, LLC·1 product·🇺🇸 United States

MICROTARGETING GUIDELINE 4000

FDA registration

FHC, INC.·1 product·🇺🇸 United States

LANX FACET SCREW SYSTEM

FDA registration

MICROPULSE INC·1 product·🇺🇸 United States

Mendell

FDA registration

Mendell·1 product·🇺🇸 United States

Olive Branch Distribution Center

FDA registration

Olive Branch Distribution Center·1 product·🇺🇸 United States

NGInstruments, Inc dba Avalign Cutting Instruments

FDA registration

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

Freedom PNS System: External Transmitter and Two Component Implanted Neurostimulator with Electrode Array and Receiver

FDA registration

CURONIX LLC·1 product·🇺🇸 United States

MR4 Laser

FDA registration

MEDICAL QUANT USA·1 product·🇺🇸 United States

Synergy Health AST, SRL

FDA registration

Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica

Plate, Bone

FDA classification

FDA Class 2 ·Plate, Bone

LANX FACET SCREW SYSTEM

FDA 510(k)

FDA Unclassified ·Unknown

MICROTARGETING GUIDELINE 4000

FDA 510(k)

FDA Class 2 ·Neurology

Electrode, Depth

FDA classification

FDA Class 2 ·Electrode, Depth

System, Facet Screw Spinal Device

FDA classification

FDA Unclassified ·System, Facet Screw Spinal Device