FDA 510(k)

IPD 閃爍空白

K 號：K253253 · 2026-01-22

申請人Implant Protesis Dental 2004, S.L.

決定日期2026-01-22

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

IPDmilled Blanks is the device name listed in this FDA 510(k) record. The listed applicant is Implant Protesis Dental 2004, S.L.. It received FDA 510(k) clearance on 2026-01-22 under 510(k) number K253253. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the IPDmilled Blanks?

IPDmilled Blanks is a medical device that received FDA 510(k) clearance on 2026-01-22. The listed applicant is Implant Protesis Dental 2004, S.L.. The 510(k) number is K253253.

When did IPDmilled Blanks receive FDA 510(k) clearance?

IPDmilled Blanks received FDA 510(k) clearance on 2026-01-22, under 510(k) number K253253.

Who is the listed applicant for IPDmilled Blanks?

The FDA 510(k) record lists Implant Protesis Dental 2004, S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPDmilled Blanks?

The FDA product code for IPDmilled Blanks is NHA.

其他以 Implant Protesis Dental 2004, S.L. 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。

K251471IPD 齿科植體基座 K242819IPD 齿科植體基座 K240570IPD 齿科植體基座 K231413IPD 齿科植體基座 K222215IPD 齿科植體基座

相關器械（代碼：NHA）

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。

K262207固定式加長基座Unidental Co., Ltd.K260940貝拉特克條ZimVie US Corp, LLC K253999通用基座 ASC 接合；通用基座 ASC 非接合；通用基座 MUA ASC；臨時基座接合和非接合；恢復基座極锥連接；Omnigrip臨床螺釘鈦金；Omnigrip假牙螺釘Nobel Biocare AB K261147Neodent植牙系統 - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLC K260061生物地平線 CEREC 兼容 Ti-BasesBioHorizons Implant Systems, Inc.

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。