植入物，皮肤，用于美容用途
PMA编号：P030050 · 2026-09-17
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申请人Q-Med AB
决定日期2026-09-17
PMA 编号P030050
产品代码LMH
设备分类第3类
医疗专科U
咨询委员会SU
请注意，您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
器械摘要
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.
常见问题
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.
谁是用于美容用途的植入、皮肤植入物的列名申请人？
The FDA 510(k) record lists Q-Med AB as the applicant. This does not by itself establish the device manufacturer.
什么是用于美容用途的皮肤植入物的FDA产品代码？
FDA产品代码为植入、皮肤用、美容用途的植入物是LMH。
相关临床试验
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官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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