Best Way to Tell the Difference between LFGB and FDA Food Silicone Products

When it comes to evaluating silicone material quality specifications, there is always a confusion between LFGB and FDA.

In this guide, we are going to compare LFGB grade silicone and FDA silicone. It explores every standard, and stipulated regulatory requirements.

Let’s dive right in:

What are LFGB Food Silicone Products?

These are abbreviated as Lebensmittel-, Bedarfsgegenstände und Futtermittelgesetz, which is a German law concerning food and food contact materials. It makes sure that silicone has to pass various tests where it is associated with food.

And for those who need a ‘European’ seal of assurance that you can cook worry-free, this is it!

Silicone Structure
Silicone Structure

What are FDA Food Silicone Products?

FDA food silicone products are produced according to the rules and regulations of the U.S. Food and Drug Administration.

Such standards help to regulate the usage of silicone in appliances that come into contact with food items, and it is not toxic in any way. You have to check if products conform to FDA standards so as not to introduce dangerous chemicals into your food.

Understanding LFGB and FDA standards

LFGB Standard

The LFGB standard is implemented in Germany and the European Union. This means you must make sure that your silicone products conform to these stringent policies. Usually this is critical if you wish to penetrate these markets.

The testing methods include migration tests for the ability of a material to release dangerous substances into food.

They cycle these silicone products to test for the migration of dangerous elements—much more rigorous than other standards.

You have to assure the safety of your products and make sure no chemicals found in them go beyond the legal limit. These tests help you know that your products are harmless and safe for use with food. As a result, making consumers trust in the high safety standards of your products.

· FDA Standard

The FDA standard works for the United States. For your silicone products to be sold in this region, you have to meet the regulations outlined below. The testing methods include migration tests that determine if hazardous substances can contaminate food.

It is necessary to inspect your products for general safety, including the fact that they do not emit chemicals in quantity. The FDA also assesses if materials are generally recognized as safe (GRAS). These procedures make it possible for you to verify if your products are safe to come into contact with food. That is if they meet the FDA’s high standards.

Comparison of LFGB and FDA Standards

Silicone Pacifier
Silicone Pacifier

· Similarities between the LFGB and FDA Regulations

These two standards will guarantee that your silicone products are fit for use with foods. For both, it is mandatory that migration tests be done to ensure that no poisonous elements transfer to the foods.

Moreover, LFGB and FDA demand the paperwork and certification to substantiate compliance as well.

· Differences in Permissible Substances and Limits

As you move between LFGB and FDA regulations, you will quickly realize differences in the allowable substances and quantities.

The criteria for LFGB regulations, apply to Germany and the EU. This exceeds the criteria for the FDA in the United States. LFGB restricts even more substances and allows for a smaller migration limit to food.

However, the FDA allows a considerably wider list of additives, as long as they are considered Generally Recognized as Safe, or GRAS.

· Variations in Testing Methodologies

There are inevitably differences in the types of tests to be performed when comparing LFGB and FDA regulations.

For Germany and the EU, LFGB testing may sometimes include more extensive and rigorous migration tests to identify even minute amounts of unsafe materials.

These tests call for you to guarantee that your products should have very low permissible limits.

On the other hand, FDA testing in the U.S. involves ensuring that the products are GRAS, which means Generally Recognized as Safe.

The FDA tests are quite rigorous but not as stringent as the LFGB tests in regard to migration limits.

Choosing Between LFGB and FDA Products

1. Factors to Consider

When comparing products certified by LFGB and FDA, it is crucial to examine the regulatory demands of your targeted market. That is, the safety standards and quality of the products with the two certifications, and the needs of consumers.

2. Regional Regulations

Some of the things you will adhere to are the rules set by the regions you intend to sell the products in. These are German and EU regulations that entail higher levels of safety requirements for baby products.

The FDA covers the United States of America, and it has different allowable substances and toxicity levels. Select the certification that is closer to the primary market you will be targeting.

3. Purpose of Silicone Products

Reflect on the application of the silicone products that you wish to produce.

For silicone products intended for long-term contact with food, using products with an LFGB safety limit might be helpful. For recreational uses, FDA-approved products may suffice.

4. Practical Implications

The choice of certification impacts the possibilities of production and commercialization in a practical way. Of course, LFGB certification entails more testing as well as higher production costs. Of course, this guarantees safety.

However, FDA certification can be cheaper while maintaining a high safety level, making it ideal for the U.S. market.


When it comes to silicone products, you can choose whether you want to opt for LFGB or FDA. This should be based on legal requirements, its application, and usability.

For all your quality silicone products from China, LEGENDAY is here for you.

More resources:

FDA Approved Silicone – Source: LEGENDAY


Update cookies preferences
Scroll to Top