When exporting heat-processed canned foods to the U.S. market, registering for an FCE (Food Canning Establishment) number with the FDA is a mandatory requirement. This is the first step toward obtaining FDA approval for your products to clear customs and enter the U.S. However, the registration process involves multiple steps and technical requirements under the FDA’s regulatory framework. As a trusted service provider, Gplus is authorized to handle the entire registration process on behalf of your business, ensuring accuracy, speed, and compliance with FDA regulations.
What is FCE?
FCE stands for Food Canning Establishment, referring to the registration of facilities that manufacture shelf-stable canned foods processed through heat sterilization.

What types of products require registration?
- LACF – Low-Acid Canned Foods: These are foods with a pH greater than 4.6 and water activity (aw) above 0.85, such as canned meat, canned fish, soups, beans, and vegetables not preserved in vinegar.
- AF – Acidified Foods: These are products with an initial pH above 4.6, which is adjusted to pH 4.6 or below by adding acid (e.g., vinegar, citric acid, lactic acid). Examples include pickled vegetables and tomato sauces.
Registering for an number not only enables your products to enter the U.S. legally, but also serves as evidence of compliance with U.S. food safety regulations.
The role of FCE in exporting food to the U.S.
- Meet FDA legal requirements for exporting products to the U.S. market
- Demonstrate food safety management capability at the manufacturing facility
- Build trust with import partners and consumers, increasing opportunities to expand into international markets
How does Gplus assist clients with FCE registration?

Information collection and initial consultation
- Name and address of the food processing facility
- Type of product intended for export (e.g., pâté, sauces, thermally processed canned foods)
- General production process
Preparing documentation and data according to FDA standards
- Draft, revise, and standardize data related to the facility
- Translate technical documents into English
- Finalize the electronic application in the correct FDA format
registration on behalf of the client
Receiving and delivering the number
- Deliver the valid number to the client
- Guide proper storage and reference of the number in compliance documents
- Provide sample templates for using the FCE number in export documentation
Post-registration support and periodic updates
- Guidance on proper use of the FCE number in export forms and importer declarations
- Updates on regulatory changes from the FDA related to FCE
- Support in routine checks or information updates when the facility or product changes
What You Need to Provide
- Business license or equivalent documentation
- Facility address and contact details
- Product list intended for export
- Product images or labels (if available)

