LQZ

Device, Jaw Repositioning

Product code

LQZ

Device name

Device, Jaw Repositioning

Device class

Class 2

21 CFR

21 CFR 872.5570

Medical specialty

Dental

Marketing pathway

510(K)

Flag

Third-party review eligible

510(k) clearances (last 3 years)

1

Summaries archived here

0 (direct download)

510(k) clearances (all years, FDA)

27 (all years; only the last 3 years are listed here)

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2024-02-23.