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Dynamometer, Ac-Powered
FDA product code LBB · Class 2 · Orthopedic
22
Registered devices
0
Adverse events
2
Recalls
36
510(k) clearances
Devices with this code
ActivForce 2 — ActivBody, Inc.microfet handgrip — Hoggan Scientific L.L.C.microfet3 — Hoggan Scientific L.L.C.KForce Bubble — KINVENT BIOMECANIQUEInnobyte Full-Arch Mouthpiece Sensor — Kube Innovation IncKINVENT — KINVENT HELLASKINVENT — KINVENT HELLASInnobyte Bilateral Clinical Package — Kube Innovation IncKINVENT — KINVENT HELLASSR-3053 — RED OAK INSTRUMENTS, LLCmicroFET Pinch — Hoggan Scientific L.L.C.AcroPinch™ Device — AXOGEN CORPORATIONInnobyte Bilateral Mouthpiece Replacement — Kube Innovation IncKForce Muscle Controller — KINVENT BIOMECANIQUEKForce Grip — KINVENT BIOMECANIQUEInnobyte Clinical Package — Kube Innovation IncAcroGrip™ Device — AXOGEN CORPORATIONKForce Link — KINVENT BIOMECANIQUESR-3053 — RED OAK INSTRUMENTS, LLCEforto — UniwebKINVENT — KINVENT HELLASmicrofet2 — Hoggan Scientific L.L.C.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-11-30 | Activbody, 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 |
| 2021-11-30 | Activbody, 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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