Learning More About FDA-Approved PEMF Devices
The Food and Drug Administration (FDA) approved PEMF devices from PEMF.inc have long been used to aid an individual’s health progression. In fact, pulsed electromagnetic field therapy got its approval to help nonunion fractures in 1979.
As such, it is essential to learn more about the FDA’s role in regulating these machines for us to have a clearer understanding of their safety.
What Is the Food and Drug Administration (FDA)?
The Food and Drug Administration (FDA) is a government agency established in 1906 that helps protect public health. It ensures that all food, medicines, healthcare devices, and other products are safe for public consumption or use. Additionally, the agency can administer laws and implement policies designed to keep the public safe from the spread of disease and harm.
Moreover, the FDA regulates the development of new drugs and medical devices while ensuring that they are effective and don’t pose risks to both humans and animals. Products under the FDA’s control or regulation don’t go on the market without their approval.
Another aspect of the FDA’s scope of responsibility is helping to speed up necessary innovations to advance public health. It is also their duty to provide the people with the science-based information needed to understand more about foods and medical products that will help shape their overall well-being.
The FDA’s Function in a Nutshell
Here’s a list of what the agency does to help protect public health:
- Evaluate products, including iMRS PEMF therapy devices, and test them to ensure they are effective, safe, and high-quality.
- Set standards in manufacturing, labelling, and advertising of the products, then regulate them to make sure they comply with the regulations.
- Monitor the product’s safety even after it is introduced to the market. Through this, the FDA can recall products or take action once they show negative effects or the public reports adverse results.
- Inspect and investigate products to ensure their compliance with the applicable laws and policies.
- Educate the public about safety and efficacy of different products in the market, which may include but are not limited to food, medicine, and medical devices.
- Share valuable information with other government agencies and organisations so they can apply the best practices when regulating certain products.
- Develop and update policies when deemed necessary.
What Products Does the FDA Regulate?
In this section, let us dig deeper into the different products regulated by the FDA.
Medical Devices
Hospitals and other healthcare facilities use medical devices to facilitate a patient’s treatment. That is why it is important to have a regulating body that oversees these machines. The FDA investigates medical devices like stents and mechanical heart valves.
The agency is also responsible for ensuring the safety, quality, and efficacy of iMRS machines and other devices designed to aid people in achieving optimal health.
Drugs and Medicines
As mentioned in this blog, the FDA also regulates the development of new drugs and develops rules to govern clinical trials. These medicines don’t only mean pills and tablets. They also include vaccines, monoclonal antibodies, and gene therapies.
Recommended by Experts
It is common for massage therapists, chiropractors, and integrated doctors to recommend the use of PEMF machines to help improve a person’s bone and overall health. What’s good about this approach is it is non-drug and non-invasive, like other bone surgeries, which also involve anesthesia and taking medications.
It is also crucial to bear in mind that your body has an existing energy flow, which is pivotal for functioning tissues and organs—PEMF uses your body’s energy to benefit you.
Food
Overall, the FDA bears no responsibility for regulating poultry and livestock. However, they can approve or reject food and colour additives. With that, the manufacturers of such additives must provide the agency with the needed information showing the safety of these substances. The FDA will only review the results and check if they comply with the specifications and restrictions.
Tobacco Products
It is an established fact that tobacco products aren’t safe for your health, and they aren’t effective either. However, the FDA sees to it that tobacco manufacturers follow the rules in alerting their market about the risks of using the product.
Also, the FDA oversees the production of other things that contain nicotine, like vape and nicotine patches.
Medicines for Animals
Aside from medicines for humans, the FDA also has jurisdiction over prescriptions for animals. Therefore, drug companies must obtain the approval of the FDA before they introduce or sell the drug to the market. On the other hand, the agency should inspect the labels of these drugs.
Nevertheless, other goods or products consumed by animals don’t need regulation from the FDA—including pet food and treats.
Get FDA-Approved PEMF Devices at PEMF.Inc Today!
Needless to say, approval from the Food and Drug Administration is one of the things you should look into when buying PEMF therapy devices. Doing so will help you ensure that you are using a safe product.
Fortunately, PEMF.inc only offers FDA-approved PEMF devices to our clients. We also have obtained approval from other agencies and organisations, including the MDSAP, ISO, Health Canada and Australia, MDC, and IEC.
Feel free to browse our page if you want to learn more about the benefits of these therapy devices. You may also call us at 0414644120 (Australia) or +61-414644120 (international) for more details.
