FDA 510(k)

Byte Aligner System

K 號：K230199 · 2023-10-18

決定日期2023-10-18

產品代碼NXC

諮詢委員會DE

決定相當於

器材摘要

Byte Aligner System is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona, Inc.. It received FDA 510(k) clearance on 2023-10-18 under 510(k) number K230199. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Byte Aligner System?

Byte Aligner System is a medical device that received FDA 510(k) clearance on 2023-10-18. The listed applicant is Dentsply Sirona, Inc.. The 510(k) number is K230199.

When did Byte Aligner System receive FDA 510(k) clearance?

Byte Aligner System received FDA 510(k) clearance on 2023-10-18, under 510(k) number K230199.

Who is the listed applicant for Byte Aligner System?

FDA 510(k) 記錄將 Dentsply Sirona, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Byte Aligner System?

The FDA product code for Byte Aligner System is NXC.

其他以 Dentsply Sirona, Inc. 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：NXC）

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。

K260527臉部4D調整器Avinent Implant System S.L.U.K260788斯麥麗歐正畸器Smylio, Inc.K260722SureSmile Aligner (ASSY500020)Dentsply Sirona, Inc.K253282ZSmile系統Dror Orthodesign , Ltd.K251454清齊正齊器（SCF-3348）Beame Medical Technology (Shenzhen) Limited K250739Primeprint直接對齊器Dreve Dentamid GmbH

官方來源

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