FDA 510(k)

LW UCLA 牙槽橋

K 號：K231235 · 2023-09-15

決定日期2023-09-15

產品代碼NHA

諮詢委員會DE

決定相當於

器材摘要

LW UCLA Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Ossvis Co., Ltd.. It received FDA 510(k) clearance on 2023-09-15 under 510(k) number K231235. 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 LW UCLA Abutment?

LW UCLA Abutment is a medical device that received FDA 510(k) clearance on 2023-09-15. The listed applicant is Ossvis Co., Ltd.. The 510(k) number is K231235.

When did LW UCLA Abutment receive FDA 510(k) clearance?

LW UCLA Abutment received FDA 510(k) clearance on 2023-09-15, under 510(k) number K231235.

Who is the listed applicant for LW UCLA Abutment?

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

What is the FDA product code for LW UCLA Abutment?

The FDA product code for LW UCLA Abutment is NHA.

其他以 Ossvis Co., Ltd. 為申請人之記錄

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