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FDA 510(k)

Star E900 Electric System

K-Number: K251701 · 2026-01-12

Decision Date2026-01-12
Product CodeEBW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Star E900 Electric System is a medical device manufactured by Dentalez, Inc., Stardental Division. It received FDA 510(k) clearance on 2026-01-12 under approval number K251701. The device is classified under product code EBW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Star E900 Electric System?

Star E900 Electric System is a medical device that received FDA 510(k) clearance on 2026-01-12. It is manufactured by Dentalez, Inc., Stardental Division. The 510(k) number is K251701.

When was Star E900 Electric System approved by the FDA?

Star E900 Electric System received FDA 510(k) clearance on 2026-01-12, under approval number K251701.

What company makes Star E900 Electric System?

Star E900 Electric System is manufactured by Dentalez, Inc., Stardental Division.

What is the FDA product code for Star E900 Electric System?

The FDA product code for Star E900 Electric System is EBW.

Related Clinical Trials

Other Devices by Dentalez, Inc., Stardental Division

Related Devices (Code: EBW)

Official Source

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