FDA 510(k)

GenesisZr 4Y+ (ST1100) 鈇化鋁

K 號：K201915 · 2021-02-23

決定日期2021-02-23

產品代碼EIH

諮詢委員會DE

決定相當於

器材摘要

GenesisZr 4Y+ (ST1100) Zirconia is the device name listed in this FDA 510(k) record. The listed applicant is United Dental Resources Corporation. It received FDA 510(k) clearance on 2021-02-23 under 510(k) number K201915. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the GenesisZr 4Y+ (ST1100) Zirconia?

GenesisZr 4Y+ (ST1100) Zirconia is a medical device that received FDA 510(k) clearance on 2021-02-23. The listed applicant is United Dental Resources Corporation. The 510(k) number is K201915.

When did GenesisZr 4Y+ (ST1100) Zirconia receive FDA 510(k) clearance?

GenesisZr 4Y+ (ST1100) Zirconia received FDA 510(k) clearance on 2021-02-23, under 510(k) number K201915.

Who is the listed applicant for GenesisZr 4Y+ (ST1100) Zirconia?

The FDA 510(k) record lists United Dental Resources Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GenesisZr 4Y+ (ST1100) Zirconia?

The FDA product code for GenesisZr 4Y+ (ST1100) Zirconia is EIH.

其他以 United Dental Resources Corporation 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。

K201608GenesisZr UHT700 鈇化鎵 K182642GenesisZr™ 4Y 齒鹼

相關器械（代碼：EIH）

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。

K262074任何-錫科斯Mediclus Co., Ltd.K262239Obsidian® 压克力壓克力超過鎂鋁Prismatik Dentalcraft, Inc.K261046牙醫用氧化鋁陶瓷空白片及上色液Hunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy陶瓷染色及釉料Zima International Inc., dba Dandy K260918佐立隆尼士Amann Girrbach AG K260859羅塞塔SM，羅塞塔SPHass Corp.

官方來源

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