FDA 510(k)

Ti-one 101 TS 齿科植體系統

K 號：K172821 · 2018-06-11

決定日期2018-06-11

產品代碼DZE

諮詢委員會DE

決定相當於

器材摘要

Ti-one 101 TS Dental Implant System is the device name listed in this FDA 510(k) record. The listed applicant is Hung Chun Bio-S Co., Ltd.. It received FDA 510(k) clearance on 2018-06-11 under 510(k) number K172821. 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 Ti-one 101 TS Dental Implant System?

Ti-one 101 TS Dental Implant System is a medical device that received FDA 510(k) clearance on 2018-06-11. The listed applicant is Hung Chun Bio-S Co., Ltd.. The 510(k) number is K172821.

When did Ti-one 101 TS Dental Implant System receive FDA 510(k) clearance?

Ti-one 101 TS Dental Implant System received FDA 510(k) clearance on 2018-06-11, under 510(k) number K172821.

Who is the listed applicant for Ti-one 101 TS Dental Implant System?

The FDA 510(k) record lists Hung Chun Bio-S Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ti-one 101 TS Dental Implant System?

The FDA product code for Ti-one 101 TS Dental Implant System is DZE.

其他以 Hung Chun Bio-S Co., 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。

K151362HC脊椎系統

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。

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官方來源

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