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

ProAdjuster Kidz — Neuromechanical Innovations, L.L.C.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONActivator Methods — Activator Methods International, Ltd.Activator Methods — Activator Methods International, Ltd.CAT Pro Select — JTECH MedicalPulStar — Sense Technology, Inc.KDY-ST — Sigma Instruments, Inc.Activator Methods — Activator Methods International, Ltd.Impulse Adjusting Instrument — Neuromechanical Innovations, L.L.C.Original CAT — JTECH MedicalActivator Methods — Activator Methods International, Ltd.Activator Methods — Activator Methods International, Ltd.ProAdjuster SRT — Neuromechanical Innovations, L.L.C.Activator Methods — Activator Methods International, Ltd.Prosports 360 — Neuromechanical Innovations, L.L.C.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONCAT EX — JTECH MedicalProsoft GT — Neuromechanical Innovations, L.L.C.Prosoft SRT — Neuromechanical Innovations, L.L.C.Activator Methods — Activator Methods International, Ltd.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONImpulse iQ Adjusting Instrument — Neuromechanical Innovations, L.L.C.KDY2 — Sigma Instruments, Inc.KDY1 — Sigma Instruments, Inc.

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.