Curajel™ 口腔凝胶
K号: K260126 · 2026-06-15
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器械摘要
Curajel™ Oral Gel is the device name listed in this FDA 510(k) record. The listed applicant is USpharma, Ltd.. It received FDA 510(k) clearance on 2026-06-15 under 510(k) number K260126. The device is classified under product code OLR. FDA Decision: Substantially Equivalent.
常见问题
What is the Curajel™ Oral Gel?
Curajel™ Oral Gel is a medical device that received FDA 510(k) clearance on 2026-06-15. The listed applicant is USpharma, Ltd.. The 510(k) number is K260126.
When did Curajel™ Oral Gel receive FDA 510(k) clearance?
Curajel™ Oral Gel received FDA 510(k) clearance on 2026-06-15, under 510(k) number K260126.
Who is the listed applicant for Curajel™ Oral Gel?
The FDA 510(k) record lists USpharma, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Curajel™ Oral Gel?
The FDA product code for Curajel™ Oral Gel is OLR.
相关临床试验
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相关器械（代码：OLR）
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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