Product code LXJ— Physical Medicine
Vera
- Classification name
- Interactive Rehabilitation Exercise Devices
- Device class
- Class 2
- Regulation
- 21 CFR 890.5360
- Advisory panel
- Physical Medicine
- Total cleared
- 27
- First cleared
- Most recent
Market context for product code LXJ
FDA has cleared devices under product code LXJ between 1981 and 2019, filed by 21 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
last 15 years- 2019
- 2018
- 2017
- 2016
- 2015
- 2014
- 2009
- 2004
- 2003
- 1998
- 1995
- 1993
- 1991
- 1989
- 1988
Top applicants under product code LXJ
Recent clearances under product code LXJ
- K192474 — VERA
- K182333 — Vera
- K180880 — DARI Health
- K171547 — Qualisys Clinical System
- K173931 — MindMotion(TM) GO
- K172882 — UINCARE HOME
- K162748 — MindMotionPRO
- K163245 — Virtual Occupational Therapy Application (VOTA)
- K151955 — YuGo System
- K150462 — Vera
- K151446 — Recovr Rehabilitation System
- K143034 — Jintronix
- K131660 — SMART (SMART-D, SMART-DX)
- K130847 — JINTRONIX REHABILITATION SYSTEM (JRS)
- K091000 — KNEEKG
- K033514 — CODA CX1 MOTION ANALYSIS SYSTEM
- K030714 — PEAK MOTUS
- K982425 — CODA MPX30 MOTION ANALYSIS SYSTEM
- K943430 — CERVICAL FUNCTION INDICATOR
- K923033 — THE TRACKER
- K924512 — LIDO V-TAK
- K911416 — ELITE SYSTEM
- K890074 — SPINETRAK
- K890075 — FOOTTRAK
- K890076 — ORTHOTRAK
- K880631 — 2K-QDA MOTION/GAIT ANALYSIS SYSTEM
- K811172 — VICON
Data sourced from openFDA. This site is unofficial and independent of the FDA.