Illusion Aligner Pro: Illusion Aligner FLX
K号: K233356 · 2024-08-08
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决定日期2024-08-08
产品代码NXC
咨询委员会DE
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器械摘要
Illusion Aligner Pro: Illusion Aligner FLX is the device name listed in this FDA 510(k) record. The listed applicant is Laxmi Dental Export Pvt., Ltd.. It received FDA 510(k) clearance on 2024-08-08 under 510(k) number K233356. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Illusion Aligner Pro: Illusion Aligner FLX?
Illusion Aligner Pro: Illusion Aligner FLX is a medical device that received FDA 510(k) clearance on 2024-08-08. The listed applicant is Laxmi Dental Export Pvt., Ltd.. The 510(k) number is K233356.
When did Illusion Aligner Pro: Illusion Aligner FLX receive FDA 510(k) clearance?
Illusion Aligner Pro: Illusion Aligner FLX received FDA 510(k) clearance on 2024-08-08, under 510(k) number K233356.
Who is the listed applicant for Illusion Aligner Pro: Illusion Aligner FLX?
The FDA 510(k) record lists Laxmi Dental Export Pvt., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Illusion Aligner Pro: Illusion Aligner FLX?
The FDA product code for Illusion Aligner Pro: Illusion Aligner FLX is NXC.
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相关器械（代码：NXC）
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。
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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