Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

turbodent touch

K-Number: K251425 · 2025-05-09

Decision Date2025-05-09
Product CodeKOJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

turbodent touch is a medical device manufactured by Mectron S.P.A.. It received FDA 510(k) clearance on 2025-05-09 under approval number K251425. The device is classified under product code KOJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the turbodent touch?

turbodent touch is a medical device that received FDA 510(k) clearance on 2025-05-09. It is manufactured by Mectron S.P.A.. The 510(k) number is K251425.

When was turbodent touch approved by the FDA?

turbodent touch received FDA 510(k) clearance on 2025-05-09, under approval number K251425.

What company makes turbodent touch?

turbodent touch is manufactured by Mectron S.P.A..

What is the FDA product code for turbodent touch?

The FDA product code for turbodent touch is KOJ.

Other Devices by Mectron S.P.A.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.