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FDA 510(k)

Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants

K 號:K251205 · 2025-11-21

決定日期2025-11-21
產品代碼NHA
諮詢委員會DE
決定相當於

器材摘要

Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona. It received FDA 510(k) clearance on 2025-11-21 under 510(k) number K251205. 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 Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants?

Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants is a medical device that received FDA 510(k) clearance on 2025-11-21. The listed applicant is Dentsply Sirona. The 510(k) number is K251205.

When did Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants receive FDA 510(k) clearance?

Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants received FDA 510(k) clearance on 2025-11-21, under 510(k) number K251205.

Who is the listed applicant for Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants?

FDA 510(k) 記錄將 Dentsply Sirona 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants?

The FDA product code for Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants is NHA.

相關臨床試驗

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其他以 Dentsply Sirona 為申請人之記錄

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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。

官方來源

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