KOJ

Airbrush

Product code
KOJ
Device name
Airbrush
Device class
Class 2
21 CFR
21 CFR 872.6080
Medical specialty
Dental
Marketing pathway
510(K)
Flag
Third-party review eligible
510(k) clearances (last 3 years)
1
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
48 (all years; only the last 3 years are listed here)

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

Last three years. Most recent: 2025-05-09.

NumberDecision dateApplicantDevice nameSummary
K2514252025-05-09Mectron S.P.A.turbodent touchPDF

1 summaries are archived here for direct download.

Official FDA classification page: KOJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).