Controversy Surrounding Development of E-cigarette-like Devices for Medical Conditions

Aug.12.2024
Controversy Surrounding Development of E-cigarette-like Devices for Medical Conditions
Several US companies developing e-cigarette-like devices for medical conditions face scrutiny from health officials and the public.

According to a recent report by Reuters, several American companies developing devices similar to e-cigarettes to alleviate medical conditions such as migraines and respiratory diseases continue to face skepticism from health authorities and the public. These companies believe that there is still a long way to go before obtaining approval from health departments, and during this period, they will need to demonstrate the effectiveness of their devices.


It has been reported that Qnovia and MIIST Therapeutics have developed nebulizer devices similar to existing medical nebulizers. These devices convert e-liquid medication into aerosol form for inhalation. Additionally, Greentank has claimed to have developed a new device aimed at addressing safety issues with existing nebulizer devices, which can more effectively treat conditions such as migraines. Experts, including Professor Federico Buonocore, a specialist in pulmonary drug delivery at Kingston University in the UK, believe that these advancements in nebulizer technology will greatly benefit patients.


The existing inhalation drug delivery devices are bulky and difficult to operate, often leading to improper use. Designs similar to e-cigarettes can address these challenges.


These companies claim that inhalation can provide faster pain relief with fewer side effects compared to pills. Inhalation therapy can relieve pain within seconds and has fewer side effects than traditional medications. However, the potential harmful effects of inhalation devices are currently hindering the progress of these projects.


According to data from the World Health Organization, approximately three billion people worldwide suffer from migraines. In addition, there are millions of people suffering from asthma or lung diseases that require inhalation medication. The World Health Organization has stated that e-cigarettes may produce harmful chemicals such as formaldehyde and heavy metals, and the long-term effects are still unclear.


Qnovia and MIIST plan to market their products as smoking cessation aids, available through prescription sales. Greentank, on the other hand, will be using their heating element chips for recreational cannabis and nicotine-containing vapor devices. Currently, Greentank is seeking pharmaceutical partners to support the development of their medication management heating element chips.


Qnovia company plans to submit a drug application in the United States soon and is planning to submit an application to the United Kingdom in 2026, with clinical trials expected to begin in September.


According to reports, tobacco companies such as Philip Morris International (PMI) had previously attempted to enter this market but were unsuccessful. Health officials pointed out numerous cases of failed inhalation devices and health issues.


The CEO of Philip Morris International (PMI) stated that the company did not meet its goals last year because it had been overly optimistic about the market acceptance of non-nicotine industries. A inhalable aspirin product developed by the company was also deemed ineffective after clinical trials last year.


We welcome news tips, article submissions, interview requests, or comments on this piece.

Please contact us at info@2firsts.com, or reach out to Alan Zhao, CEO of 2Firsts, on LinkedIn


Notice

1.  This article is intended solely for professional research purposes related to industry, technology, and policy. Any references to brands or products are made purely for objective description and do not constitute any form of endorsement, recommendation, or promotion by 2Firsts.

2.  The use of nicotine-containing products — including, but not limited to, cigarettes, e-cigarettes, nicotine pouchand heated tobacco products — carries significant health risks. Users are responsible for complying with all applicable laws and regulations in their respective jurisdictions.

3.  This article is not intended to serve as the basis for any investment decisions or financial advice. 2Firsts assumes no direct or indirect liability for any inaccuracies or errors in the content.

4.  Access to this article is strictly prohibited for individuals below the legal age in their jurisdiction.

 

Copyright

 

This article is either an original work created by 2Firsts or a reproduction from third-party sources with proper attribution. All copyrights and usage rights belong to 2Firsts or the original content provider. Unauthorized reproduction, distribution, or any other form of unauthorized use by any individual or organization is strictly prohibited. Violators will be held legally accountable.

For copyright-related inquiries, please contact: info@2firsts.com

 

AI Assistance Disclaimer

 

This article may have been enhanced using AI tools to improve translation and editorial efficiency. However, due to technical limitations, inaccuracies may occur. Readers are encouraged to refer to the cited sources for the most accurate information.

We welcome any corrections or feedback. Please contact us at: info@2firsts.com

U.S. House Defense Bill Includes Pilot Review of Vapes, Nicotine Pouches and Heated Tobacco for Military Smokers
U.S. House Defense Bill Includes Pilot Review of Vapes, Nicotine Pouches and Heated Tobacco for Military Smokers
On July 23, 2026, the U.S. House of Representatives passed its version of the Fiscal Year 2027 National Defense Authorization Act (NDAA), which includes Section 707 provisions requiring the Department of Defense to evaluate tobacco use and nicotine alternatives among military personnel. The pilot program would examine products including vapes, nicotine pouches and heated tobacco products, primarily among active-duty service members who continue using combustible tobacco. The provision is a policy evaluation effort, not an authorization for military vaping promotion or a ban on vape products.
Jul.28
PMI’s ZYN Launches Loyalty Platform in Mexico, Tapping World Cup Viewing Scenes for Nicotine Pouch Marketing
PMI’s ZYN Launches Loyalty Platform in Mexico, Tapping World Cup Viewing Scenes for Nicotine Pouch Marketing
PMI’s nicotine pouch brand ZYN has launched the ZYN Club loyalty platform in Mexico and introduced ZYN Live Stadium viewing experiences around football matches, showing how nicotine pouch brands are using rewards, limited benefits and offline consumption settings to reach adult consumers.
Jun.29
Hunan China Tobacco Industry files heated tobacco device patent featuring adult-user identification through pressure sensing
Hunan China Tobacco Industry files heated tobacco device patent featuring adult-user identification through pressure sensing
China-based Hunan China Tobacco Industry Co., Ltd. and Shenzhen Baisha Technology Co., Ltd. have filed a patent application covering an adult-user identification mechanism for heated tobacco devices. The patent proposes using flexible pressure sensors installed in the device grip area to collect pressure distribution patterns generated when users hold the device. The system evaluates factors including effective contact area, grip shape and contact duration, and combines roller movement detection to determine whether unlocking conditions are met. The filing reflects exploration of device-level user recognition and smarter interaction technologies for heated tobacco products (HTPs).
Aug.05
Senate Democrat Wyden Probes Trump Administration Vape Policy Shift, Seeks Records From HHS and Reynolds American
Senate Democrat Wyden Probes Trump Administration Vape Policy Shift, Seeks Records From HHS and Reynolds American
U.S. Senator Ron Wyden, the Democratic ranking member of the Senate Finance Committee, has launched an investigation into flavored vape policy changes and requested records from the Department of Health and Human Services (HHS), Reynolds American and Botanic Tonics. The investigation focuses on a timeline involving Reynolds American’s $5 million donation to MAGA Inc. in April 2026 and subsequent vape policy developments. Wyden said the review aims to examine potential links between political donations, corporate communications and government decisions. The investigation does not represent a finding of wrongdoing.
Innovation
Aug.07 by 2Firsts Perspectives
EU Trade Department Faces Scrutiny Over Contacts With Tobacco Industry
EU Trade Department Faces Scrutiny Over Contacts With Tobacco Industry
European Ombudswoman Teresa Anjinho has opened an inquiry into how the European Commission’s Directorate-General for Trade handles interactions with the tobacco industry. The case follows a complaint from a civil society organisation that alleges regular, unnecessary and non-transparent contacts between DG TRADE and tobacco industry representatives, raising questions over compliance with the EU’s obligations under the WHO Framework Convention on Tobacco Control. The inquiry remains ongoing, and the Ombudswoman has not reached any finding of maladministration.
Aug.24
Nearly Half of Seoul Vape Vending Machines Bypassed by Fake IDs, Raising Youth Access Concerns
Nearly Half of Seoul Vape Vending Machines Bypassed by Fake IDs, Raising Youth Access Concerns
Seoul city authorities inspected 339 tobacco vending machines at e-cigarette retailers and found that 168, or 49.5%, allowed purchases using fake IDs, showing that unmanned retail terminals and adult-verification systems remain a major enforcement gap after e-cigarettes were brought under tobacco regulation.
Market
Jul.03 by 2Firsts Perspectives