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FDA 510(k)

BASE290 LED Curing Light

K-Number: K233518 · 2023-11-02

Decision Date2023-11-02
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BASE290 LED Curing Light is a medical device manufactured by Handpiece Headquarters. It received FDA 510(k) clearance on 2023-11-02 under approval number K233518. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BASE290 LED Curing Light?

BASE290 LED Curing Light is a medical device that received FDA 510(k) clearance on 2023-11-02. It is manufactured by Handpiece Headquarters. The 510(k) number is K233518.

When was BASE290 LED Curing Light approved by the FDA?

BASE290 LED Curing Light received FDA 510(k) clearance on 2023-11-02, under approval number K233518.

What company makes BASE290 LED Curing Light?

BASE290 LED Curing Light is manufactured by Handpiece Headquarters.

What is the FDA product code for BASE290 LED Curing Light?

The FDA product code for BASE290 LED Curing Light is EBZ.

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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.