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FDA 510(k)

Dentsply Sirona Titanium Bases system

K-Number: K250295 · 2025-04-30

ApplicantDentsply Sirona
Decision Date2025-04-30
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Dentsply Sirona Titanium Bases system is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2025-04-30 under approval number K250295. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dentsply Sirona Titanium Bases system?

Dentsply Sirona Titanium Bases system is a medical device that received FDA 510(k) clearance on 2025-04-30. It is manufactured by Dentsply Sirona. The 510(k) number is K250295.

When was Dentsply Sirona Titanium Bases system approved by the FDA?

Dentsply Sirona Titanium Bases system received FDA 510(k) clearance on 2025-04-30, under approval number K250295.

What company makes Dentsply Sirona Titanium Bases system?

Dentsply Sirona Titanium Bases system is manufactured by Dentsply Sirona.

What is the FDA product code for Dentsply Sirona Titanium Bases system?

The FDA product code for Dentsply Sirona Titanium Bases system is NHA.

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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.

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