FDA 510(k)

Tetric plus 填充劑；Tetric plus 流動劑

K 號：K261485 · 2026-07-01

決定日期2026-07-01

產品代碼EBF

諮詢委員會DE

決定相當於

器材摘要

Tetric plus Fill;Tetric plus Flow is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2026-07-01 under 510(k) number K261485. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tetric plus Fill;Tetric plus Flow?

Tetric plus Fill;Tetric plus Flow is a medical device that received FDA 510(k) clearance on 2026-07-01. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K261485.

When did Tetric plus Fill;Tetric plus Flow receive FDA 510(k) clearance?

Tetric plus Fill;Tetric plus Flow received FDA 510(k) clearance on 2026-07-01, under 510(k) number K261485.

Who is the listed applicant for Tetric plus Fill;Tetric plus Flow?

The FDA 510(k) record lists Ivoclar Vivadent, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tetric plus Fill;Tetric plus Flow?

The FDA product code for Tetric plus Fill;Tetric plus Flow is EBF.

其他以 Ivoclar Vivadent, 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。

K253953IPS e.max 鑫瓷 K252450Adhese 2 K233995Ivotion 基礎列印機 K153753TelioCAD 多功能醫療設備

相關器械（代碼：EBF）

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。

K262982Core·it雙用式醫療設備規範文本Spident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695流動性修復材質（KP-Flow LF，KP-Flow MF，KP-Flow HF）Guilin Kevin Peter Technology Co., Ltd.K262228超越大量填充濃縮複合材料Ultradent Products, Inc.K261246SRGC-06GC America, Inc.K261093DIAFILDiaDent Group International

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。