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)

Nucleoss T6 Dental Implant System

K-Number: K192062 · 2020-08-27

Decision Date2020-08-27
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Nucleoss T6 Dental Implant System is a medical device manufactured by Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST. It received FDA 510(k) clearance on 2020-08-27 under approval number K192062. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nucleoss T6 Dental Implant System?

Nucleoss T6 Dental Implant System is a medical device that received FDA 510(k) clearance on 2020-08-27. It is manufactured by Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST. The 510(k) number is K192062.

When was Nucleoss T6 Dental Implant System approved by the FDA?

Nucleoss T6 Dental Implant System received FDA 510(k) clearance on 2020-08-27, under approval number K192062.

What company makes Nucleoss T6 Dental Implant System?

Nucleoss T6 Dental Implant System is manufactured by Sanlilar Tibbi Cihazlar Medikal Kimya Sanayi Ticaret Ltd. ST.

What is the FDA product code for Nucleoss T6 Dental Implant System?

The FDA product code for Nucleoss T6 Dental Implant System is DZE.

Related Clinical Trials

Related PubMed Literature

Related Devices (Code: DZE)

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.