IMPLANT，抗胃食管反流
PMA编号：P100049 · 2026-01-16
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决定日期2026-01-16
PMA 编号P100049
产品代码LEI
设备分类第3类
医疗专科U
咨询委员会GU
请注意，由于您只提供了“GU”这个词，我无法提供完整的翻译。如果您能提供完整的句子或段落，我将能够为您提供准确的翻译。
器械摘要
IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX is the device name listed in this FDA 510(k) record. The listed applicant is Torax Medical. It received FDA 510(k) clearance on 2026-01-16. The device is classified under product code LEI. It was reviewed by the GU advisory panel.
常见问题
What is the IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX?
IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX is a medical device that received FDA 510(k) clearance on 2026-01-16. The listed applicant is Torax Medical.
When did IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX receive FDA 510(k) clearance?
The clearance date for IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX can be found in the official FDA records.
谁是IMPLANT，抗胃食管反流产品的列名申请人？
The FDA 510(k) record lists Torax Medical as the applicant. This does not by itself establish the device manufacturer.
IMPLANT, ANTI-GASTROESOPHAGEAL REFLUX 的 FDA 产品代码是什么？
FDA产品代码为IMPLANT，反胃食管反流产品的代码是LEI。
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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