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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 the device name listed in this FDA 510(k) record. The listed applicant is Handpiece Headquarters. It received FDA 510(k) clearance on 2023-11-02 under 510(k) 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. The listed applicant is Handpiece Headquarters. The 510(k) number is K233518.

When did BASE290 LED Curing Light receive FDA 510(k) clearance?

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

Who is the listed applicant for BASE290 LED Curing Light?

The FDA 510(k) record lists Handpiece Headquarters as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Handpiece Headquarters as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: EBZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.