Kinematic Knee

FDA registration

HOWMEDICA OSTEONICS CORP·1 product·🇺🇸 United States

KINEMATIC II REPLACEMENT TIBIAL INSERTS

FDA 510(k)

FDA Class 2 ·Orthopedic

moorLDI2-BI

FDA registration

MOOR INSTRUMENTS LTD.·2 products·🇬🇧 United Kingdom

ALTUS PARTNERS

FDA registration

ALTUS PARTNERS·1 product·🇺🇸 United States

Acero Precision

FDA registration

Acero Precision·1 product·🇺🇸 United States

proprietary

FDA registration

CULVER TOOL & ENGINEERING·1 product·🇺🇸 United States

SAMS 8000

FDA registration

TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·3 products·🇺🇸 United States

Wheelchair Elevator

FDA registration

SAVARIA CONCORD LIFTS INC.·1 product·🇨🇦 Canada

Century

FDA registration

Century HLM, LLC·1 product·🇺🇸 United States

MOORLD12-B1 LASER DOPPLER BURNS IMAGER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Altus Spine Interbody Fusion System

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Probe, Blood-Flow, Extravascular

FDA classification

FDA Class 2 ·Probe, Blood-Flow, Extravascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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