turbodent touch— 510(k) K251425

Substantially Equivalent

Mectron S.P.A.

FDA 510(k) clearance K251425 for turbodent touch, Substantially Equivalent on 2025-05-09. Applicant: Mectron S.P.A.. Device class: 2.

Clearance details

Applicant: Mectron S.P.A.
Product code: Code KOJ
Device class: Class 2
Regulation: 21 CFR 872.6080
Advisory panel: Dental
Date received: 2025-05-08
Decision date: 2025-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carasco, IT

Download summary PDF View on FDA.gov ↗

Recent devices under product code KOJ

K063236 — BETA-POWDER2007-02-16
K042872 — RONDOFLEX PLUS 3602004-11-23
K033675 — PROSMILE AIR POLISHER AND PROPHYLAXIS POWDER2004-01-15
K033215 — PREPAIR2004-01-09
K024105 — VELOPEX AQUACUT FLUID ABRASION UNIT2003-10-09

More clearances from Mectron S.P.A.

K242432 — MT-Bone2024-08-19
K231391 — Combi Touch2023-05-15
K171326 — Piezosurgery White2018-04-13
K171958 — PIEZOSURGERY TOUCH, PIEZOSURGERY WHITE2018-01-12
K153743 — PIEZOSURGERY PLUS2016-05-25

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