ID LIGHT 照明系统
K号: K250804 · 2025-06-04
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决定日期2025-06-04
产品代码EBD
咨询委员会DE
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决定实质等同
器械摘要
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.
常见问题
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.
相关临床试验
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相关器械（代码：EBD）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
K254091GLOSSY COAT (15ML)YAMAHACHI DENTAL MFG., Co.K240735visio.lign 颜色，visio.lign 防护罩Bredent GmbH & Co. KGK223365RODIN自然化套件Belport Company, Inc., Gingi-PakK211854VITA Akzent LCVita Zahnfabrik GmbH H Rauter & COK162408表面纳米清漆，Plaquit，LightpaintDreve Dentamid GmbHK163568SHOFU 树脂釉Shofu Dental Corporation
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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