Bonvadis®
K号: K251093 · 2025-06-09
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器械摘要
Bonvadis® is the device name listed in this FDA 510(k) record. The listed applicant is Oneness Biotech Co., Ltd.. It received FDA 510(k) clearance on 2025-06-09 under 510(k) number K251093. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Bonvadis®?
Bonvadis® is a medical device that received FDA 510(k) clearance on 2025-06-09. The listed applicant is Oneness Biotech Co., Ltd.. The 510(k) number is K251093.
When did Bonvadis® receive FDA 510(k) clearance?
Bonvadis® received FDA 510(k) clearance on 2025-06-09, under 510(k) number K251093.
Who is the listed applicant for Bonvadis®?
The FDA 510(k) record lists Oneness Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bonvadis®?
The FDA product code for Bonvadis® is FRO. This falls under the Anesthesiology category.
相关临床试验
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列明Oneness Biotech Co., Ltd.为申报人的其他记录
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。
相关器械（代码：FRO）
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。
K254168Actolind®（06.3637. Actolind®凝胶加强型）ACTO GmbHK254041SkinSmart 抗菌保湿凝胶Magic Science Supply, LLCK261646Redermax® 抗菌伤口基质Beijing Kreate Medical Co., Ltd.K253665Vashe Plus 抗菌溶液Urgo Medical North America, LLCK251929SilverCeuticals® 抗菌伤口凝胶Silverceuticals, Inc.K261023Microdacyn 伤口冲洗溶液Sonoma Pharmaceuticals, Inc.
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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