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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 a medical device manufactured by Id Korea Co., Ltd.. It received FDA 510(k) clearance on 2025-06-04 under approval 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. It is manufactured by Id Korea Co., Ltd.. The 510(k) number is K250804.

When was ID LIGHT CURE SYSTEM approved by the FDA?

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

What company makes ID LIGHT CURE SYSTEM?

ID LIGHT CURE SYSTEM is manufactured by Id Korea Co., Ltd..

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

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

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