Document intake

Compliance document center

Use this page to share FCC, RoHS, CE, factory ISO, and FDA-related files for the exact PBM helmet models you want to publish.

FDA wording will stay conservative until you provide the exact registration, listing, clearance, or approval documents that support the public claim.

Send compliance files with RFQ Email compliance pack

What to send

PDF or image file of each certificate, declaration, or report
Exact model names covered by the document
Issue date and expiration date
Issuing body, laboratory, or certification authority
Whether the file can be public, partner-only, or internal only
Any exact wording restrictions for website publication

How it will be used

Public product pages will link to the relevant compliance file when approved
Sales teams can use the page as a trust and due-diligence hub
The site will only publish FDA wording that matches the actual document scope
Documents can be attached to product pages, RFQ response kits, or a password-protected asset pack later

Product compliance

FCC documentation

Reserved for FCC test reports, grant/listing details, applicable standards, product model coverage, test lab information, and validity notes.

Pending document upload

Certificate or report numberCovered model namesTest standardTesting laboratoryIssue datePDF or image file

Files can be attached later

FCC documentation can be shared for covered OEM projects after the exact model and test report scope are confirmed.

Product compliance

RoHS documentation

Reserved for RoHS declarations, material compliance reports, restricted-substance testing, and model coverage details.

Pending document upload

Declaration or report numberCovered models and materialsApplicable RoHS directive or standardTesting laboratoryIssue datePDF or image file

Files can be attached later

RoHS documentation is prepared and reviewed by model and production scope before partner publication.

Product compliance

CE technical documentation

Reserved for CE declaration materials, EMC/LVD references, photobiological safety files, model coverage, and supporting test reports.

Pending document upload

Declaration numberCovered model namesApplicable directives and standardsTesting laboratory or notified body if applicableIssue dateDeclaration and report files

Files can be attached later

CE-related materials are available for selected models and should be matched to the target market and OEM configuration.

Factory system

Factory ISO documentation

Reserved for ISO certificates, factory quality-system scope, audit information, validity period, and issuing certification body.

Pending document upload

ISO standard, such as ISO 9001 or ISO 13485Certificate numberCertified company or factory nameScope of certificationIssuing bodyValid from / valid untilCertificate file

Files can be attached later

Factory ISO information will be listed with certificate number, scope, issuing body, and validity period after document review.

Market access

FDA-related information

Reserved for FDA registration/listing, owner/operator details, device listing information, 510(k) references if any, or other applicable US market-access materials.

Pending document review

Exact FDA status typeRegistration, listing, or 510(k) reference if applicableCovered company and device namesProduct code or classification if applicableValid date or listing yearSupporting screenshot or PDF

Files can be attached later

FDA-related wording will be published only after the exact document type is confirmed. The site will not state FDA approval unless formal approval/clearance documents support that wording.