Product code LXV— Unknown
BALANCE REHABILITATION UNIT (BRU)
- Classification name
- Apparatus, Vestibular Analysis
- Device class
- Unclassified
- Advisory panel
- Unknown
- Total cleared
- 22
- First cleared
- Most recent
Market context for product code LXV
FDA has cleared devices under product code LXV between 1977 and 2022, filed by 19 applicant companies. No FDA device recalls reference this product code.
Clearances per year
last 15 years- 2022
- 2020
- 2019
- 2018
- 2012
- 2010
- 2009
- 2008
- 2007
- 1998
- 1992
- 1991
- 1989
- 1987
- 1985
Top applicants under product code LXV
Recent clearances under product code LXV
- K220231 — GyroStim
- K200529 — Orion
- K192652 — TRV
- K183661 — ClearEdge Balance System
- K190735 — EQ Balance
- K173669 — K-D Balance
- K121590 — VESTIBULAR ANALYSIS APPARATUS
- K102364 — NYDIAG 200
- K082634 — VERTIGONE BPPV GOGGLE
- K081602 — DIZZYFIX
- K071973 — EPLEY OMNIAX
- K070676 — KOREBALANCE (KINESTHETIC ABILITY TRAINER)
- K070085 — BALANCE REHABILITATION UNIT (BRU)
- K971549 — VMT SYSTEM
- K922037 — SYSTEM 2000, ROTATIONAL VESTIBULAR CHAIR
- K911795 — KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)
- K891008 — VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
- K884926 — BALANCE SYSTEM
- K872093 — RVT-50 ROTARY CHAIR FOR VESTIBULAR TESTING
- K851744 — EQUITEST
- K781268 — CHAIR, VESTIBULAR, ROTARY, COMPUT.
- K771618 — COMPUTERIZED POSTURE PLATFORM
Data sourced from openFDA. This site is unofficial and independent of the FDA.