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FDA 510(k)

諾里斯醫療牙植體系統 - 外板

K 號:K210852 · 2022-06-24

決定日期2022-06-24
產品代碼DZE
諮詢委員會DE
決定相當於

器材摘要

Noris Medical Dental Implants System - Cortical is the device name listed in this FDA 510(k) record. The listed applicant is Noris Medical , Ltd.. It received FDA 510(k) clearance on 2022-06-24 under 510(k) number K210852. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Noris Medical Dental Implants System - Cortical?

Noris Medical Dental Implants System - Cortical is a medical device that received FDA 510(k) clearance on 2022-06-24. The listed applicant is Noris Medical , Ltd.. The 510(k) number is K210852.

When did Noris Medical Dental Implants System - Cortical receive FDA 510(k) clearance?

Noris Medical Dental Implants System - Cortical received FDA 510(k) clearance on 2022-06-24, under 510(k) number K210852.

Who is the listed applicant for Noris Medical Dental Implants System - Cortical?

The FDA 510(k) record lists Noris Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Noris Medical Dental Implants System - Cortical?

The FDA product code for Noris Medical Dental Implants System - Cortical is DZE.

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其他以 Noris Medical , Ltd. 為申請人之記錄

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相關器械(代碼:DZE)

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。

官方來源

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