FDA 510(k)

Velmeni for Dentists (V4D) 根管牙周

K号: K252953 · 2026-05-11

决定日期2026-05-11

产品代码MYN

咨询委员会RA

决定实质等同

器械摘要

Velmeni for Dentists (V4D) Endo-Perio is the device name listed in this FDA 510(k) record. The listed applicant is Velmeni, Inc.. It received FDA 510(k) clearance on 2026-05-11 under 510(k) number K252953. The device is classified under product code MYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Velmeni for Dentists (V4D) Endo-Perio?

Velmeni for Dentists (V4D) Endo-Perio is a medical device that received FDA 510(k) clearance on 2026-05-11. The listed applicant is Velmeni, Inc.. The 510(k) number is K252953.

When did Velmeni for Dentists (V4D) Endo-Perio receive FDA 510(k) clearance?

Velmeni for Dentists (V4D) Endo-Perio received FDA 510(k) clearance on 2026-05-11, under 510(k) number K252953.

Who is the listed applicant for Velmeni for Dentists (V4D) Endo-Perio?

FDA 510(k)记录将Velmeni, Inc.列为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Velmeni for Dentists (V4D) Endo-Perio?

The FDA product code for Velmeni for Dentists (V4D) Endo-Perio is MYN.

列明Velmeni, Inc.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。

K254096VELMENI为牙医（V4D）3D K250753VELMENI 为牙医（V4D）K240003Velmeni牙科医生专用（V4D）

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。