• Skip to primary navigation
  • Skip to main content
  • +1-757-224-0177
  • Contact Us
  • MyFDA Login
  • COVID-19 PPE
  • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • 中文
    • Portuguese
    • 日本語
Registrar

Registrar

Assistance with U.S. FDA Regulations

  • English
    • Español
    • Italiano
    • Deutsch
    • Français
    • 中文
    • Portuguese
    • 日本語
  • FDA Registration
  • Services
    • FDA Registration
    • Cosmetics FDA Registration
    • U.S. FDA Detention Assistance
    • Food Safety and FSMA
    • FDA Labeling
    • UDI and GUDID
    • Master Files
    • GACC Registration
    • Unique Facility Identifier (UFI)
    • U.S. FDA Export Certificate Requirements
    • TTB Registration
  • Products
    • FDA Compliance Monitor
      • Buyer Insights
      • Marketplace
      • Exporter Marketplace
    • Cosmetri
    • A la Calc
    • Online Training
  • Our Brands
    • Cosmetri
    • A la Calc
  • Industries
    • Food and Beverages
    • Dietary Supplements
    • Medical Devices
    • Drugs
    • Cosmetics
    • Other
  • Resources
    • Resources
    • Regulatory News
    • Events / Webinars
    • Partners
    • Free Tools
  • About Us
    • About
    • Contact Us
    • Careers

FCE-SID Requirements

U.S. FDA Food Canning Establishment (FCE) Registration & Process Filings (SID)

Facilities that manufacture, process, or package foods intended for consumption in the United States are required to register in the FDA Food Facility Registration (FFR) system. Companies that produce certain Acidified and Low-Acid Canned Food (LACF) packaged in hermetically sealed containers are also required to obtain a Food Canning Establishment (FCE) registration. A facility’s FCE registration must be linked to its FFR, and the data in the two registrations must match

Additionally, LACF and acidified food facilities must submit unique filings for each process used during production. Each of these “Process Filings” is assigned a unique Submission Identifier (SID) number.

Get Expert Assistance Today

Complete this form for assistance with FDA FCE registration and process filing requirements

  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • Provide your company information

  • This field is hidden when viewing the form
  • This field is hidden when viewing the form
  • Food Safety

    Is your Food Safety Plan FDA-Compliant?

    U.S. FDA requires most types of registered food facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) Plans. A HARPC plan must follow unique standards mandated by U.S. FDA. Other food safety systems may not completely satisfy FDA requirements.

  • Food Safety

    U.S. FDA requires most types of registered food facilities to implement Hazard Analysis and Risk-Based Preventive Controls (HARPC) Plans. A HARPC plan must follow unique standards mandated by U.S. FDA. Other food safety systems may not completely satisfy FDA requirements.

  • Food Label Deadline

    Deadline Approaching for FDA's New Label Rules

    Many food companies have less than 12 months to update their labeling to comply with new FDA labeling rules. The new rules include updates to the nutrition facts chart, serving sizes, mandatory declarations, and more.

  • Food Label Deadline

    Labeling mistakes result in more than 22% of all detentions in the United States.

    Many companies do not realize their labels are non-compliant until their products are detained, which may result in delays, re-labeling expenses, or destruction of inventory. Help avoid costly issues in port. Have Registrar Corp's experts assess the FDA compliance of your labels.

  • Drop files here or
    Max. file size: 50 MB.
    • Drop files here or
      Max. file size: 50 MB.
      • NOTE: Registrar Corp cannot verify or recover your registration without:

        • Your Registration Number and PIN
        • or
        • your FURLS Login and Password.

        If you do not have either set of information, we encourage you to re-register.

        Re-Register Now
      • This field is hidden when viewing the form
      • (11 Digit Number)
      • (Please indicate capital letters)
      • Compliance Information

      •  
      • Drop files here or
        Max. file size: 50 MB.
        • Drop files here or
          Max. file size: 50 MB.
          • Max. file size: 15 MB.
          • Max. file size: 15 MB.
          • Drop files here or
            Max. file size: 15 MB, Max. files: 10.
            • Drop files here or
              Max. file size: 15 MB.
              • Drop files here or
                Max. file size: 15 MB.
                • Drop files here or
                  Max. file size: 15 MB.
                  • Drop files here or
                    Max. file size: 15 MB.

                    • Provide the following information for each of your NIOSH approved respirators
                      Manufacturer NameModel NumberNIOSH Approval Number 
                    • Drop files here or
                      Max. file size: 50 MB.
                      • Issued by another regulatory authority or conformity assessment body. Include the authorization number and name of the assessment body (if applicable)
                        Drop files here or
                        Max. file size: 50 MB.
                        •  
                          Drop files here or
                          Max. file size: 50 MB.
                          • Report should demonstrate applicable performance standards have been met
                            Drop files here or
                            Max. file size: 50 MB.

                            Is My Product Considered Acidified or Low Acid?

                            A food product is typically considered an Acidified or Low Acid food if it is packaged in a hermetically sealed container, has a water activity of 0.85 or above, and is not stored, distributed, and retailed under refrigerated conditions. If the food has a final equilibrium pH less than or equal to 4.6, the food is Acidified. If the food has a final equilibrium pH greater than 4.6, the food is Low Acid.

                            Common examples of foods subject to FDA’s FCE and SID requirements include canned tuna, canned roasted red peppers, and coconut water

                             Determining if your product is subject to FCE-SID requirements can be difficult.

                            Registrar Corp’s team of specialists can help you comply with FCE requirements, determine if your product is considered an Acidified or Low Acid food, assist with FCE registration, and provide guidance on the required elements, formats, and particularities of SID submissions.

                            FCE Wizard

                            DETERMINE IF YOUR PRODUCT IS SUBJECT TO FCE-SID REQUIREMENTS

                            Easily determine if your products may be subject to FDA FCE-SID requirements by using Registrar Corp’s free FCE Wizard

                            Get Started

                            Expert Tip: By answering a few simple questions, the Wizard can generate a report indicating possible requirements based on factors such as pH, water activity, and ingredients.

                             Lookup an SID

                            CONFIRM IF AN EXISTING SID IS VALID

                            Verify whether SIDs are currently in FDA’s database by using Registrar Corp’s free SID Lookup tool

                            Get Started

                            Expert Tip: Manufacturers, importers, and brokers will find this tool especially helpful, as they must ensure the firms they represent comply with all registration and process filing requirements.

                            Solutions

                            FDA Registration

                            FDA Compliance Monitor

                            FDA Labeling

                            View All

                            About

                            About Us

                            Resources

                            Free Tools

                            Fees

                            Contact Us

                             

                            Reviews

                            Locations

                            Events

                            Associations

                            Careers

                            Phone: +1-757-224-0177

                            Fax: +1-757-224-0179

                            [email protected]

                            © 2025 Registrar Corp

                            144 Research Drive Hampton, Virginia 23666 USA
                            Terms of Use | Privacy Policy

                            • English
                              • Español
                              • Italiano
                              • Deutsch
                              • Français
                              • 中文
                              • Portuguese
                              • 日本語
                              • Back
                            • FDA Registration
                            • Services
                              • FDA Registration
                              • Cosmetics FDA Registration
                              • U.S. FDA Detention Assistance
                              • Food Safety and FSMA
                              • FDA Labeling
                              • UDI and GUDID
                              • Master Files
                              • GACC Registration
                              • Unique Facility Identifier (UFI)
                              • U.S. FDA Export Certificate Requirements
                              • TTB Registration
                              • Back
                            • Products
                              • FDA Compliance Monitor
                                • Buyer Insights
                                • Marketplace
                                • Exporter Marketplace
                                • Back
                              • Cosmetri
                              • A la Calc
                              • Online Training
                              • Back
                            • Our Brands
                              • Cosmetri
                              • A la Calc
                              • Back
                            • Industries
                              • Food and Beverages
                              • Dietary Supplements
                              • Medical Devices
                              • Drugs
                              • Cosmetics
                              • Other
                              • Back
                            • Resources
                              • Resources
                              • Regulatory News
                              • Events / Webinars
                              • Partners
                              • Free Tools
                              • Back
                            • About Us
                              • About
                              • Contact Us
                              • Careers
                              • Back

                            FDA has cancelled thousands of registrations that were not properly renewed or did not include
                            an accurate Unique Facility Identifier (UFI). If you need immediate assistance, Registrar Corp can help.

                            Notice: Medical Device and Drug establishments that did not renew their FDA registrations in   must re-register.


                            Get Help Now

                            FDA-registered facilities must renew their registrations by December 31,  

                            Medical Device and Drug establishments must renew their registrations by December 31,  

                            Renew Now

                            Reminder

                            The U.S. Food and Drug Administration (FDA) requires that all registered food, medical device, and drug facilities renew their FDA registration between October 1 and December 31,

                            Renew Now

                            Notice

                            The U.S. FDA Registration Renewal period CLOSED on December 31,

                            If you did not renew by the deadline, you must re-register with FDA.

                            Re-register or verify that your registration was renewed for :

                            Re-Register
                            Verify

                            Limited Time Offer

                            Get 18 Months of Registration and U.S. Agent service for the price of 12 when you sign up today.

                            Get Started
                            Open Modal