DeviceClearance

Product code LQZ— Dental

ADJUSTABLE PM POSITIONER

Classification name
Device, Jaw Repositioning
Device class
Class 2
Regulation
21 CFR 872.5570
Advisory panel
Dental
Total cleared
27
First cleared
Most recent

Market context for product code LQZ

FDA has cleared 27 devices under product code LQZ between 1987 and 2024, filed by 22 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

Top applicants under product code LQZ

Recent clearances under product code LQZ

Data sourced from openFDA. This site is unofficial and independent of the FDA.