EMC China Lab

Differences Between FDA and LFGB for Food Contact Materials

Views :
Update time : 2025-12-23

Food Contact Materials (FCM) refer to materials that come into direct contact with food during the normal use of products. These materials include, but are not limited to, plastics, rubber, resins, silica gel, metals, alloys, paper, cardboard, glass, ceramics, enamel, colorants, printing inks, etc. They are widely used in fields such as food packaging, tableware, kitchen utensils, food processing machinery, and kitchen electrical products.

 

Differences Between FDA and LFGB for Food Contact Materials(图1)


What is FDA Registration

FDA is the abbreviation of the U.S. Food and Drug Administration, an executive agency established under the U.S. Department of Health and Human Services and the Public Health Service. Its main responsibilities include the supervision and inspection of products such as food, drugs, medical devices, food additives, cosmetics, etc.

 

What is LFGB Certification

lfgb certification, also known as the Law on the Regulation of Food, Tobacco Products, Cosmetics and Other Daily Necessities, is the most important basic legal document in Germany's food hygiene management system. It serves as the guideline and core for formulating other special food hygiene laws and regulations.

 

Differences Between FDA and LFGB

1. Regional Application Differences

FDA registration pertains to food certification in the United States, while LFGB certification applies to food-related certification in Germany. The two sets of standards follow the respective national regulations, with no overlap between them, forming completely independent systems.

2. Differences in Testing Items

Article 30 and Article 31 of Germany's LFGB stipulate the following testing items:

1. Initial inspection of samples and materials;

2. Sensory evaluation of odor and taste transfer;

3. Plastic samples: Testing of transferable components and leachable heavy metals;

4. Metals: Testing of composition and leachable heavy metals;

5. Silicone resins: Testing of transferable or volatile organic compounds;

6. Special materials, etc.

FDA registration covers different testing items as follows:

7. Overall migration test: Determining the amount of harmful substances migrating from materials to food under specific temperature and contact duration conditions that simulate real food contact scenarios;

2. Heavy metal migration test: Measuring the migration limits of heavy metals (such as lead, cadmium, chromium, arsenic, mercury, etc.) from materials to food;

3. Volatile organic compound (VOC) migration test: Testing the migration limits of volatile organic compounds from materials to food;

4. Specific substance migration test: Setting specific migration limits for certain substances, including heavy metals and volatile organic compounds.

 

3. Differences in Testing Content

A key feature of FDA certification is that it only measures the total amount of migrated substances, without detecting specific migrated components.

In contrast, LFGB certification not only tests the total migrated amount but also detects the migration amount of individual monomers.

 

4. Differences in Testing Conditions

For aqueous solution media:

① Under FDA standards, the limit specified in 21 CFR 2600 is relatively high, making it easier to pass the test, while compliance with 21 CFR 1810 is more challenging.

② LFGB testing for aqueous solutions is generally easy to pass, but the test using isooctane as the medium is comparatively difficult.

• 

Notes on LFGB Certification

The key difference between Germany's LFGB and other food-grade testing standards lies in its comprehensive testing requirements, which are stricter than those of most other countries. Moreover, LFGB test results are more accurate, which is why LFGB Test Reports are widely recognized and accepted by other countries around the world.


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
Mandatory Standard for Portable Power Banks GB 473 Mandatory Standard for Portable Power Banks GB 473
04 .12.2026
New mandatory GB 47372-2026 standard strengthens portable power bank safety through stricter cell te...
ISO 10993-10 In Vitro Skin Sensitization Test Serv ISO 10993-10 In Vitro Skin Sensitization Test Serv
04 .11.2026
In vitro skin sensitization tests assess allergic risks for safety use. JJR LAB offers ISO 10993-10 ...
What is ISO 10993 Biocompatibility Testing? What is ISO 10993 Biocompatibility Testing?
04 .11.2026
JJR is a CNAS- and ISO/IEC 17025-accredited Laboratory providing ISO 10993 compliance testing. Repor...
How to Perform a Valid CCK-8 Cytotoxicity Assay How to Perform a Valid CCK-8 Cytotoxicity Assay
04 .10.2026
A valid CCK-8 cytotoxicity assay uses WST-8 to assess cell viability via color change, with key step...
Introduction to Cytotoxicity Assay (CCK-8 Method) Introduction to Cytotoxicity Assay (CCK-8 Method)
04 .10.2026
CCK-8 assay measures viable cells via WST-8 conversion, enabling rapid, sensitive detection for drug...
What Are the Cytotoxicity Assay Methods? What Are the Cytotoxicity Assay Methods?
04 .10.2026
Cytotoxicity assays reveal cell safety by measuring viability or damage. JJR LAB outlines methods li...
What is Ingress Protection (IP) Testing and Standa What is Ingress Protection (IP) Testing and Standa
04 .08.2026
Ingress Protection (IP) defines enclosure resistance to dust and water per IEC 60529; JJR LAB verifi...
What is UL 153 Lighting Standards and Portable Lum What is UL 153 Lighting Standards and Portable Lum
04 .08.2026
UL 153 defines safety rules for portable luminaires; Amazon requires compliant testing. JJR verifies...

Leave Your Message