FDA 510(k)

牙醫s-Clean SQ-SL 裝置

K 號：K240511 · 2024-05-20

決定日期2024-05-20

產品代碼DZE

諮詢委員會DE

決定相當於

器材摘要

Dentis s-Clean SQ-SL Fixture is the device name listed in this FDA 510(k) record. The listed applicant is Dentis Co., Ltd.. It received FDA 510(k) clearance on 2024-05-20 under 510(k) number K240511. 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 Dentis s-Clean SQ-SL Fixture?

Dentis s-Clean SQ-SL Fixture is a medical device that received FDA 510(k) clearance on 2024-05-20. The listed applicant is Dentis Co., Ltd.. The 510(k) number is K240511.

When did Dentis s-Clean SQ-SL Fixture receive FDA 510(k) clearance?

Dentis s-Clean SQ-SL Fixture received FDA 510(k) clearance on 2024-05-20, under 510(k) number K240511.

Who is the listed applicant for Dentis s-Clean SQ-SL Fixture?

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

What is the FDA product code for Dentis s-Clean SQ-SL Fixture?

The FDA product code for Dentis s-Clean SQ-SL Fixture is DZE.

其他以 Dentis 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。

K253493牙醫SQ-SL AXEL固定器 K241065ChecQ (AC100)K233921Luvis 椅子 (LC700C)K241063s-Clean 扫描修復基座 K233544MESHEET 注意：此文本中未提供具体的医疗设备名称或相关监管文本，因此无法进行翻译。请提供具体的文本内容以便进行翻译。K230126牙醫s-Clean標準牙根擴張體

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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。

K261392三活牙植體系統Paragon Implant Mfg., LLC K260463ZEROS 齿科植體系統Zeros Co., Ltd.K251188UNIQA® 齿科植體系統Uniqa Dental, Ltd.K251232MegaGen 遺傳子顎骨牙植體系統Megagen Implant Co., Ltd.K250806牙齒植體系統A.B. Dental Devices , Ltd.K260006INOS系統Inosys, Inc.

官方來源

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