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FDA 510(k)

Rennou™ 漆光劑(3% / 薄荷);Rennou™ 漆光劑(3% / 草莓);Rennou™ 漆光劑(3% / 樱桃);Rennou™ 漆光劑(3% / 气球糖)

K 號:K243777 · 2025-05-27

申請人Theodent, LLC
決定日期2025-05-27
產品代碼LBH
諮詢委員會DE
決定相當於

器材摘要

Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum) is the device name listed in this FDA 510(k) record. The listed applicant is Theodent, LLC. It received FDA 510(k) clearance on 2025-05-27 under 510(k) number K243777. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum)?

Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum) is a medical device that received FDA 510(k) clearance on 2025-05-27. The listed applicant is Theodent, LLC. The 510(k) number is K243777.

When did Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum) receive FDA 510(k) clearance?

Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum) received FDA 510(k) clearance on 2025-05-27, under 510(k) number K243777.

Who is the listed applicant for Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum)?

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

What is the FDA product code for Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum)?

The FDA product code for Rennou™ Varnish (3% / Spearmint); Rennou™ Varnish (3% / Strawberry); Rennou™ Varnish (3% / Cherry); Rennou™ Varnish (3% / Bubble Gum) is LBH.

相關臨床試驗

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相關器械(代碼:LBH)

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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