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FDA 510(k)

ID LIGHT CURE SYSTEM

K-Number: K250804 · 2025-06-04

ApplicantId Korea Co., Ltd.
Decision Date2025-06-04
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ID LIGHT CURE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Id Korea Co., Ltd.. It received FDA 510(k) clearance on 2025-06-04 under 510(k) number K250804. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ID LIGHT CURE SYSTEM?

ID LIGHT CURE SYSTEM is a medical device that received FDA 510(k) clearance on 2025-06-04. The listed applicant is Id Korea Co., Ltd.. The 510(k) number is K250804.

When did ID LIGHT CURE SYSTEM receive FDA 510(k) clearance?

ID LIGHT CURE SYSTEM received FDA 510(k) clearance on 2025-06-04, under 510(k) number K250804.

Who is the listed applicant for ID LIGHT CURE SYSTEM?

The FDA 510(k) record lists Id Korea Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ID LIGHT CURE SYSTEM?

The FDA product code for ID LIGHT CURE SYSTEM is EBD.

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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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