The Official Resource for ISO 12312-2 Solar Eye Safety Standards Eclipse Events: August 2026 (Europe)  |  February 2027 (Americas)

Before You Begin

We verify that manufacturers meet all ISO 12312-2 requirements—not just transmittance. Products must demonstrate compliance with the complete standard including uniformity, material quality, mounting, and labeling requirements.

This is not a certification service. We are an independent verification resource that reviews your existing test documentation and certifications. We do not perform testing ourselves.

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No Fee for Listing Verification is free
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Same Standards for All Including our own products
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Documentation Kept Confidential We don't share your files
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Basic Requirements (All Markets)

Every manufacturer must provide documentation demonstrating compliance with the complete ISO 12312-2 standard. This applies regardless of where you sell your products.

Required Documentation

  • ISO 12312-2 Test Report Complete test report from an accredited laboratory covering all requirements: transmittance (UV, visible, IR), uniformity, material quality, and surface defects.
  • Laboratory Accreditation Certificate Proof that the testing laboratory is accredited by a body that is a signatory to the ILAC Mutual Recognition Arrangement (MRA).
  • Scope of Accreditation Documentation showing ISO 12312-2 testing is within the laboratory's scope of accreditation. Not all accredited labs are accredited for this specific standard.
  • Product Samples or Images Clear images of your actual products showing all labeling, warnings, manufacturer information, and care instructions as they appear on the finished product.
  • Company Information Legal company name, physical address, website, and contact information. This must match what appears on your product labeling.
⚠️ Transmittance-Only Reports Are Not Sufficient

Some laboratories offer "quick" testing that only covers transmittance requirements. We require test reports covering the complete standard. If your report only shows transmittance data, you will need to obtain additional testing.

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Additional EU Requirements

If you intend to sell in the European Union, your products must meet additional PPE Category 2 certification requirements. These are in addition to the basic requirements above.

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Required for EU Sales

The EU classifies eclipse glasses as Personal Protective Equipment (PPE) Category 2, which requires third-party certification by an EU Notified Body.

  • EU Type Examination Certificate Certificate issued by an authorized EU Notified Body confirming your product meets EN ISO 12312-2:2022 requirements.
  • Declaration of Conformity (DoC) Your formal declaration that the product meets all applicable EU requirements. Must include all elements specified in PPE Regulation (EU) 2016/425.
  • CE Marking Evidence Images showing CE marking with Notified Body number (e.g., CE 0527) as it appears on your product.
  • Language Compliance Evidence that safety information and instructions are provided in the official language(s) of your target EU markets.
📋 Each Design Requires Separate Certification

Under current EU regulations, each distinct product design requires its own EU Type Examination Certificate. Different artwork or branding on the same base product constitutes a different design. If you offer multiple designs, you'll need to provide certification for each one you want listed.

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What We Verify

Our review process checks that your documentation demonstrates compliance with the complete ISO 12312-2 standard. Here's what we look for:

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Complete Testing Test report covers all requirements—transmittance, uniformity, material quality, surface defects—not just optical properties.
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Laboratory Credentials Testing lab is accredited under ILAC MRA with ISO 12312-2 specifically in their scope of accreditation.
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Labeling Compliance Product labeling includes all required elements: manufacturer info, warnings, care instructions, and ISO reference.
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Product Matching The test report actually applies to the products you're selling, not a different variant or earlier version.
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EU Documentation (if applicable) Type Examination Certificate is from an authorized Notified Body, DoC contains all required elements.
Current Validity Certificates and accreditations are current and have not expired or been withdrawn.
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The Review Process

Once you submit your documentation, here's what to expect:

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Submit

Email your documentation package to us

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Review

We examine all documentation (typically 5-10 business days)

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Clarify

We may request additional information if needed

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Decision

Approved manufacturers are added to our verified list

🔄 Ongoing Compliance

Being listed is not permanent. We periodically review listed manufacturers and may request updated documentation. If certifications expire or we become aware of compliance issues, listings may be suspended or removed.

Our Commitment to Transparency

We believe in applying the same standards to everyone, including ourselves. Here's how we operate:

  • No payment is required or accepted for listing—this prevents conflicts of interest
  • The same verification requirements apply to all manufacturers, including Lunt Solar Systems (operated by this site's founder)
  • We do not share or sell your documentation to third parties
  • If we reject an application, we'll explain why and what would be needed for approval
  • We disclose our methodology so you know exactly what we're checking

Ready to Submit?

Compile your documentation and send it to us. Please include all required items in a single email if possible.

Submit Documentation

Please allow 5-10 business days for initial review. We'll contact you if we need additional information.

📋 Download Submission Checklist

A printable checklist of all required documentation to help you prepare your submission.

Download PDF