免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

Proimtech 齒科身體植入物,Proimtech 牙根帽,Proimtech 恢復帽,Proimtech 牙根帽螺釘

K 號:K231100 · 2024-08-23

決定日期2024-08-23
產品代碼DZE
諮詢委員會DE
決定相當於

器材摘要

Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw is the device name listed in this FDA 510(k) record. The listed applicant is Proimtech Saglik Urunleri Anonim Sirketi. It received FDA 510(k) clearance on 2024-08-23 under 510(k) number K231100. 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 Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw?

Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw is a medical device that received FDA 510(k) clearance on 2024-08-23. The listed applicant is Proimtech Saglik Urunleri Anonim Sirketi. The 510(k) number is K231100.

When did Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw receive FDA 510(k) clearance?

Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw received FDA 510(k) clearance on 2024-08-23, under 510(k) number K231100.

Who is the listed applicant for Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw?

The FDA 510(k) record lists Proimtech Saglik Urunleri Anonim Sirketi as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw?

The FDA product code for Proimtech Dental Body Implant, Proimtech Abutment, Proimtech Healing Cap, Proimtech Abutment Screw is DZE.

相關臨床試驗

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。

其他以 Proimtech Saglik Urunleri Anonim Sirketi 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。

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。

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。

↑