FDA 510(k)

Adin Customized Abutments

K 號：K250178 · 2025-10-17

決定日期2025-10-17

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

Adin Customized Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Adin Dental Implant Systems , Ltd.. It received FDA 510(k) clearance on 2025-10-17 under 510(k) number K250178. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Adin Customized Abutments?

Adin Customized Abutments is a medical device that received FDA 510(k) clearance on 2025-10-17. The listed applicant is Adin Dental Implant Systems , Ltd.. The 510(k) number is K250178.

When did Adin Customized Abutments receive FDA 510(k) clearance?

Adin Customized Abutments received FDA 510(k) clearance on 2025-10-17, under 510(k) number K250178.

Who is the listed applicant for Adin Customized Abutments?

The FDA 510(k) record lists Adin Dental Implant Systems , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Adin Customized Abutments?

The FDA product code for Adin Customized Abutments is NHA.

其他以 Adin Dental Implant Systems , Ltd. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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相關器械（代碼：NHA）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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