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Therma Bright Submits Updated FDA 510K Application Requesting Correction of Venowave Device's Intended Use, Labeling, and Description

Therma Bright Submits Updated FDA 510K Application Requesting Correction of Venowave Device's Intended Use, Labeling, and Description

Therma Bright 提交了更新的 FDA 510K 申请,要求更正 Venowave 设备的预期用途、标签和描述
newsfile ·  2023/09/07 05:30

Toronto, Ontario--(Newsfile Corp. - September 7, 2023) - Therma Bright Inc. (TSXV: THRM) (OTCQB: TBRIF) ("Therma" or the "Company"), developer and partner in a wide-range of leading-edge, proprietary diagnostic and medical device technologies, announced today the Company has submitted an updated U.S. Food and Drug Administration (FDA) 510K application to correct the Venowave device's intended use, labeling and product description in order to better address the U.S. Centers for Medicare and Medicaid Services (CMS) application for permanent Current Procedural Terminology (CPT) / Healthcare Common Procedure Coding System (HCPCS) codes.

安大略省多伦多-(Newsfile Corp.-2023年9月7日)-Therma Bright Inc.(TSXV:THRM)(OTCQB:TBRIF)(以下简称“Therma”或“公司”)今天宣布,该公司已提交最新的美国食品和药物管理局(FDA)510K申请,以纠正Venowave设备的预期用途。标签和产品说明,以便更好地满足美国医疗保险和医疗补助服务中心(CMS)对永久当前程序术语(CPT)/医疗保健通用程序编码系统(HCPCS)代码的申请。

In late August, CMS asked the Company to first secure approval from the FDA through an updated 510K application stating that the Venowave device can be used successively by multiple patients. This was a key requirement for the Company to secure in order to update its CMS application to secure the nine (9) permanent CPT and HCPCS codes.

8月下旬,CMS要求该公司首先通过更新的510K应用程序获得FDA的批准,声明Venowave设备可以被多名患者连续使用。这是该公司为了更新其CMS应用程序以确保九(9)个永久CPT和HCPCS代码的安全而需要确保的关键要求。

"Our team worked quickly to prepare this first step in updating our FDA 501K application for our Venowave device, specifically around the use, labeling and device description," shared Rob Fia, CEO of Therma Bright. "Once we secure FDA approval on our updated 510K application, our team will be ready to address the second step of updating our CMS application stating that the Venowave can be used successively by multiple patients. We are cautiously optimistic that this change, along with some other minor changes, to our updated FDA application, and subsequent CMS application, will result in a positive decision on our CPT and HCPCS codes."

Therma Bright首席执行官罗布·菲亚分享道:“我们的团队迅速准备好为我们的Venowave设备更新FDA 501k应用程序的第一步,特别是围绕使用、标签和设备描述。一旦我们确保FDA批准我们更新的510K应用程序,我们的团队将准备好处理更新我们的CMS应用程序的第二步,声明Venowave可以被多名患者连续使用。我们谨慎乐观地认为,这一变化,加上对我们更新的FDA应用程序和后续的CMS应用程序的一些其他微小变化,将导致对我们的CPT和HCPCS代码做出积极的决定。“

The Company looks forward to providing more information as it becomes available on the unique permanent CPT and HCPCS codes and on expanding its distribution partners across the U.S. for its Venowave device.

该公司期待着在获得唯一的永久CPT和HCPCS代码以及扩大其Venowave设备在美国各地的分销伙伴方面提供更多信息。

About Therma Bright Inc.
Therma Bright is a developer and partner in a wide range of leading edge, proprietary diagnostic and medical device technologies focused on providing consumers and medical professionals with quality, innovative solutions that address some of today's most important medical and healthcare challenges. Therma Bright Inc. trades on the (TSXV: THRM) (OTCQB: TBRIF) (FSE: JNX). Visit: .

关于Therma Bright Inc.
Therma Bright是一家领先的专有诊断和医疗设备技术的开发商和合作伙伴,致力于为消费者和医疗专业人员提供高质量的创新解决方案,以应对当今一些最重要的医疗和保健挑战。Therma Bright Inc.在多伦多证券交易所(TSXV:THRM)(场外交易市场代码:TBRIF)(纽约证券交易所代码:JNX)交易。参观:。

Therma Bright Inc.
Rob Fia, CEO
rfia@thermabright.com

Therma Bright Inc.
罗布·菲亚,首席执行官
邮箱:rfia@thermabright.com

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FORWARD-LOOKING STATEMENTS
Certain statements in this news release constitute "forward-looking" statements. These statements relate to future events such as the commercialization and sales of Venowave and related technology as described in the news release. All such statements involve substantial known and unknown risks, uncertainties and other factors which may cause the actual results to vary from those expressed or implied by such forward-looking statements. Forward-looking statements involve significant risks and uncertainties, they should not be read as guarantees of future performance or results, and they will not necessarily be accurate indications of whether such results will be achieved. Actual results could differ materially from those anticipated due to several factors and risks. Although the forward-looking statements contained in this news release are based upon what management of the Company believes are reasonable assumptions on the date of this news release, the Company cannot assure investors that actual results will be consistent with these forward-looking statements. The forward-looking statements contained in this press release are made as of the date hereof and the Company disclaims any intention or obligation to update or revise any forward-looking statements whether because of new information, future events or otherwise, except as required under applicable securities regulations.

前瞻性陈述
本新闻稿中的某些陈述构成“前瞻性”陈述。这些陈述涉及未来的事件,如新闻稿中描述的Venowave和相关技术的商业化和销售。所有这些陈述都涉及大量已知和未知的风险、不确定因素和其他因素,这些风险、不确定因素和其他因素可能导致实际结果与这些前瞻性陈述明示或暗示的结果大不相同。前瞻性陈述涉及重大风险和不确定因素,不应被解读为对未来业绩或结果的保证,也不一定是能否实现此类结果的准确迹象。由于几个因素和风险,实际结果可能与预期大不相同。尽管本新闻稿中包含的前瞻性陈述是基于公司管理层认为本新闻稿发布之日的合理假设,但公司不能向投资者保证实际结果将与这些前瞻性陈述一致。本新闻稿中包含的前瞻性陈述是自本新闻稿发布之日起作出的,除非适用的证券法规另有要求,否则公司不会因为新信息、未来事件或其他原因而更新或修改任何前瞻性陈述的意图或义务。

Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in the policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this press release.

多伦多证券交易所及其监管服务提供商(该术语在多伦多证券交易所的政策中定义)均不对本新闻稿的充分性或准确性承担责任。

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