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Dynamometer, Ac-Powered

FDA product code LBB · Class 2 · Orthopedic

24
Registered devices
0
Adverse events
2
Recalls
36
510(k) clearances

Devices with this code

microFET Pinch — Hoggan Scientific L.L.C.Innobyte Bilateral Clinical Package — Kube Innovation IncKINVENT — KINVENT HELLASKINVENT — KINVENT HELLASKForce Link — KINVENT BIOMECANIQUESR-3053 — RED OAK INSTRUMENTS, LLCKINVENT — KINVENT HELLASSR-3053 — RED OAK INSTRUMENTS, LLCKForce Muscle Controller — KINVENT BIOMECANIQUEKForce Grip — KINVENT BIOMECANIQUEEforto — UniwebInnobyte Clinical Package — Kube Innovation IncSAEHAN Digital Hand Dynamometer(DHD-1) — Saehan CorporationKINVENT — KINVENT HELLASActivForce 2 — ActivBody, Inc.microfet2 — Hoggan Scientific L.L.C.AcroPinch™ Device — AXOGEN CORPORATIONInnobyte Bilateral Mouthpiece Replacement — Kube Innovation IncKForce Bubble — KINVENT BIOMECANIQUEmicrofet3 — Hoggan Scientific L.L.C.Innobyte Full-Arch Mouthpiece Sensor — Kube Innovation IncSAEHAN Digital Hand Dynamometer(DHD-3) — Saehan Corporationmicrofet handgrip — Hoggan Scientific L.L.C.AcroGrip™ Device — AXOGEN CORPORATION

Recent recalls

DateFirmReason
2021-11-30Activbody, Inc.Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing
2021-11-30Activbody, Inc.Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing

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