FDA 510(k)

ID LIGHT CURE SYSTEM

Número K: K250804 · 2025-06-04

Data da decisão2025-06-04

Código do produtoEBD

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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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