FDA Device Intelligence
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Manipulator, Plunger-Like Joint

FDA product code LXM · Class U · Unknown

29
Registered devices
8
Adverse events
1
Recalls
32
510(k) clearances

Devices with this code

Activator Methods — Activator Methods International, Ltd.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONKDY-ST — Sigma Instruments, Inc.Impulse iQ Adjusting Instrument — Neuromechanical Innovations, L.L.C.ProAdjuster SRT — Neuromechanical Innovations, L.L.C.PulStar — Sense Technology, Inc.Prosports 360 — Neuromechanical Innovations, L.L.C.Activator Methods — Activator Methods International, Ltd.KDY2 — Sigma Instruments, Inc.Activator Methods — Activator Methods International, Ltd.Activator Methods — Activator Methods International, Ltd.Prosoft GT — Neuromechanical Innovations, L.L.C.KDY1 — Sigma Instruments, Inc.Activator Methods — Activator Methods International, Ltd.Impulse Adjusting Instrument — Neuromechanical Innovations, L.L.C.CAT EX — JTECH MedicalIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONCAT Pro Select — JTECH MedicalProAdjuster Kidz — Neuromechanical Innovations, L.L.C.Prosoft SRT — Neuromechanical Innovations, L.L.C.Activator Methods — Activator Methods International, Ltd.Activator Methods — Activator Methods International, Ltd.Khan Kinetic Treatment Device (KKT-M2) — Optima Health Solutions International Corporation

Recent recalls

DateFirmReason
2013-03-06Advanced Orthogonal Equipment, IncorporatedUnapproved medical device

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.