Learning Red Light Therapy
Red Light Therapy Certifications & Compliance
Review regulatory listings and conformity documents associated with selected YaMuri red light therapy models, including FDA, FCC Part 15B, EU EMC and RoHS records.
Red Light Therapy Certifications & Compliance Documents
A transparent reference center for regulatory listings and conformity documents associated with selected YaMuri red light therapy products. Check the model scope, document number, issuing or testing organization, and verification source before relying on any claim.
Scope first: Documents on this page do not automatically apply to every YaMuri product. A claim applies only when the exact model is identified in the relevant record or document.
Compliance evidence at a glance
FDA listing, FCC documentation, EU electromagnetic compatibility documentation, and RoHS documentation are different forms of evidence. They should not be combined into a single claim of “medical approval.”
| Evidence | Status | Identifier | What it supports | What it does not prove |
|---|---|---|---|---|
| U.S. FDA database | Official source verified | Class II listings Product Codes IRT, IQE and ILY |
Manufacturer registration and device listings for the product families and models named in each FDA record. | FDA approval, clearance, certification, endorsement, or clinical effectiveness. |
| FCC Part 15B | Document available | Report KTI250909F724 | Supplier’s Declaration of Conformity documentation relating to applicable radio-frequency emissions requirements. | Medical-device status, treatment safety, or therapeutic performance. |
| EU EMC | Document available | Certificate KTI250909E725C Report KTI250909E725 |
Documentation referencing the EMC Directive 2014/30/EU for listed models. | Certification under the EU Medical Device Regulation or proof of clinical benefit. |
| RoHS | Document available | Certificate KTI250909R722C Report KTI250909R722 |
Documentation addressing specified restricted substances for listed models. | Complete product-safety certification or treatment efficacy. |
| ETL | Verification pending | No official listing supplied | No ETL claim is made on this page until a model-specific Intertek listing is available. | — |
Which records apply to which product models?
Use this matrix before linking a product page to a particular compliance statement. The model name must appear in the underlying record; similarity in appearance, wavelength, or product family is not enough.
| Product family / models shown in evidence | FDA record | FCC | EU EMC | RoHS |
|---|---|---|---|---|
|
Red light therapy lamp/panel family YA20, YA21, YA22, YA23, YA24, YA25, YA26, YA27, YA28, YA30, YA60, YA120, YA180, YA240, YA360, YA480, YA600, YA720, subject to the exact spelling in each source. |
Class II; Product Code IRT; 21 CFR 890.5740 | Document shows YA60, YA120, YA180, YA240, YA360, YA480, YA600 and YA720 | Document shows the models printed on the certificate, including YA60 | Document shows the models printed on the certificate, including YA60 |
|
LED therapeutic mask family YB-series models listed in the FDA record. |
Class II; Product Code IQE | Not established by the document displayed here | Confirm against the exact certificate before making a claim | Confirm against the exact certificate before making a claim |
|
Therapeutic pad family YC-SX, YC-S, YC-M, YC-L, YC-XL, YC-XXL and YC-XXXL as shown in the FDA record. |
Class II; Product Code ILY | Not established by the document displayed here | Confirm against the exact certificate before making a claim | Confirm against the exact certificate before making a claim |
Model lists can change when records are renewed or updated. Product pages should use precise wording such as “model included in the referenced record,” rather than suggesting every YaMuri product carries every document.
FDA establishment registration and Class II device listings
The FDA Establishment Registration & Device Listing database currently shows Shenzhen Caidisen Optoelectronics Co., Ltd. as the registered manufacturer and identifies multiple YaMuri model families in Class II listings.
- Manufacturer
- Shenzhen Caidisen Optoelectronics Co., Ltd.
- Establishment number
- 3040387923
- Owner/operator number
- 10093910
- Manufacturer operation
- Manufacturer
- Panel/lamp listing
- Product Code IRT; Device Class II; 21 CFR 890.5740
- Other listed families
- Mask family under Product Code IQE and pad family under Product Code ILY, as identified in their respective records.
View the manufacturer and product-family results in the official FDA database →
View the official FDA IRT listing for the named YA-series models →
Third-party registration summary retained for reference at YaMuri’s direction. It was not issued or certified by FDA and may not reflect the newest FDA record identifiers. Use the live FDA links above for authoritative, current verification.
How to interpret the FDA evidence
- Establishment registration identifies a facility participating in regulated device activities.
- Device listing identifies device categories and proprietary names submitted under that establishment.
- Class II is a regulatory classification; it is not an FDA quality award.
- A model appearing in a listing is not the same as a device receiving FDA approval or 510(k) clearance.
Read FDA’s official registration and listing clarification →
FCC Part 15B documentation
Electromagnetic-emissions scope
The displayed Supplier’s Declaration of Conformity identifies selected YA-series models and references FCC Part 15 Subpart B and ANSI C63.4:2014.
- Applicant/manufacturer
- Shenzhen Caidisen Optoelectronics Co., Ltd.
- Report number
- KTI250909F724
- Issue date
- September 26, 2025
- Model scope
- Only the models expressly printed on the document, including YA60.
FCC documentation relates to radio-frequency emissions and electromagnetic compatibility. It is not a medical or therapeutic certification.
EU electromagnetic compatibility documentation
What this document supports
The displayed document identifies selected YaMuri models and references standards used for electromagnetic compatibility assessment under Directive 2014/30/EU.
- Certificate number
- KTI250909E725C
- Test report
- KTI250909E725
- Issue date
- September 26, 2025
- Model scope
- Only the models expressly printed on the document.
This is presented as EU EMC conformity documentation—not as certification under the EU Medical Device Regulation and not as evidence of clinical performance.
RoHS restricted-substances documentation
Materials-related scope
The displayed document references Directive 2011/65/EU, applicable amendments, and IEC 62321 test methods for specified restricted substances in electrical and electronic equipment.
- Certificate number
- KTI250909R722C
- Report number
- KTI250909R722
- Issue date
- September 26, 2025
- Model scope
- Only the models expressly printed on the document.
RoHS documentation concerns specified substance restrictions. It does not independently certify total product safety, medical performance, or treatment outcomes.
How YaMuri presents compliance evidence
Exact-model matching
We connect a claim to a product only when the corresponding record or document identifies that model.
Primary-source priority
Where an official public database exists, such as FDA’s database, the live government record takes priority over third-party summaries.
Claim-to-scope alignment
Electromagnetic compatibility, restricted-substances documentation, and regulatory listing are explained separately.
No automatic clinical claims
Compliance records do not by themselves prove clinical efficacy or guarantee individual wellness results.
Certification and compliance FAQ
Are all YaMuri products FDA approved?
No. YaMuri does not make that blanket claim. Selected product models appear in FDA Class II device listings under the manufacturer. Registration and listing are not FDA approval or clearance.
Does every document cover every model?
No. Each document has its own model scope. Check the table and the model list printed on the underlying document before applying a claim.
What does the CE document mean?
The displayed document references the EU EMC Directive. It is not presented as EU Medical Device Regulation certification.
Is every YaMuri product ETL Listed?
No ETL claim is made here. A product should be described as ETL Listed only after its model-specific Intertek listing is independently verified.
Find the documentation that matches your product
Return to the relevant product page to confirm the exact model name, then use the model-scope table above to identify the applicable records.
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