植入式，皮內，用於美容用途
PMA 核准號：P030050 · 2026-09-17
廣告
器材摘要
Implant, dermal, for aesthetic use is the device name listed in this FDA 510(k) record. The listed applicant is Q-Med AB. It received FDA 510(k) clearance on 2026-09-17. The device is classified under product code LMH. It was reviewed by the SU advisory panel.
常見問題
What is the Implant, dermal, for aesthetic use?
Implant, dermal, for aesthetic use is a medical device that received FDA 510(k) clearance on 2026-09-17. The listed applicant is Q-Med AB.
When did Implant, dermal, for aesthetic use receive FDA 510(k) clearance?
The clearance date for Implant, dermal, for aesthetic use can be found in the official FDA records.
誰是列於植入、皮膚用、美學用途的申請人？
The FDA 510(k) record lists Q-Med AB as the applicant. This does not by itself establish the device manufacturer.
FDA產品代碼是什麼？用於美容用途的皮膚植入物？
FDA產品代碼，用於美容用途的植入、皮膚類產品為LMH。
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。
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。
廣告