← Product Code [OHS](/submissions/SU/subpart-e%E2%80%94surgical-devices/OHS) · K220064
# Synergy Marble (Model: Opasm) (K220064)
_Yrs Group, Inc. · OHS · Jul 22, 2022 · General, Plastic Surgery · SESE_
**Canonical URL:** https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OHS/K220064
## Device Facts
- **Applicant:** Yrs Group, Inc.
- **Product Code:** [OHS](/submissions/SU/subpart-e%E2%80%94surgical-devices/OHS.md)
- **Decision Date:** Jul 22, 2022
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 878.4810
- **Device Class:** Class 2
- **Review Panel:** General, Plastic Surgery
- **Attributes:** Therapeutic
## Intended Use
SYNERGY MARBLE is a hand-held device for over-the counter aesthetic purposes. The device red light and amber light are intended for the use in treating wrinkles on the face, and the blue light is intended for the treatment of the mild to moderate inflammatory acne.
## Device Story
Synergy Marble is a battery-powered, hand-held LED device for OTC aesthetic use. It emits light in red (625nm), blue (465nm), and amber (605nm) spectra. The device includes an applicator, charging station, and adapter. Users apply the treatment surface directly to facial skin to treat wrinkles (red/amber light) or mild-to-moderate inflammatory acne (blue light). Treatment duration is 3 minutes per target area, twice weekly for 6 weeks. The device provides consistent light energy to the skin; it does not contain user-repairable components. It is intended for home use by the patient.
## Clinical Evidence
Bench testing only. No clinical data provided. Safety and performance were validated through testing against standards including IEC 60601-1 (electrical safety), IEC 60601-1-2 (EMC), IEC 62471 (photobiological safety), IEC 62133-2 (battery safety), and ISO 10993 series (biocompatibility: cytotoxicity, irritation, sensitization, and systemic toxicity).
## Technological Characteristics
Hand-held LED device; ABS plastic construction. Wavelengths: Red 625nm±3nm, Blue 465nm±3nm, Amber 605nm±3nm. Irradiance: Red 55.3mW/cm², Blue 48.2mW/cm², Amber 38.3mW/cm². Powered by lithium battery. Standards: ANSI AAMI ES60601-1, IEC 60601-1-2, IEC 60601-1-6, IEC 60601-1-11, IEC 62471, IEC 62133-2, ISO 10993-5, ISO 10993-10, ISO 10993-11.
## Regulatory Identification
(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.
## Predicate Devices
- Looper (Model: ZX-579S) ([K202055](/device/K202055.md))
## Reference Devices
- MMSphere™ ([K190443](/device/K190443.md))
## Submission Summary (Full Text)
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July 22, 2022
YRS Group Inc % Doris Dong Manager Shanghai CV Technology Co., Ltd. Room 903, No.19 Dongbao Road, Songjiang Area Shanghai, Shanghai 201613 China
Re: K220064
Trade/Device Name: Synergy Marble (Model: Opasm) Regulation Number: 21 CFR 878.4810 Regulation Name: Laser Surgical Instrument For Use In General And Plastic Surgery And In Dermatology Regulatory Class: Class II Product Code: OHS, OLP Dated: June 27, 2022 Received: July 5, 2022
Dear Doris Dong:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
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Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely.
Jianting Wang Acting Assistant Director DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health
Enclosure
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# Indications for Use
510(k) Number (if known) K220064
Device Name SYNERGY MARBLE
Indications for Use (Describe)
SYNERGY MARBLE is a hand-held device for over-the counter aesthetic purposes. The device red light and amber light are intended for the use in treating wrinkles on the blue light is intended for the treatment of the mild to moderate inflammatory acne.
Prescription Use (Part 21 CFR 801 Subpart D)
X Over-The-Counter Use (21 CFR 801 Subpart C)
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## 510(k) Summary [As required by 21 CFR 807.92]
### 1. Submission Information
| 510(k) Number: | K220064 |
|------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Date: | July 21, 2022 |
| Type of 510(k) Submission: | Traditional 510(k) |
| Basis for 510(k) Submission: | New device |
| Owner: | YRS Group Inc. |
| | 5151 S Procyon St, Suite 105, Las Vegas, NV 89118, US |
| | Tel: 1-702 4268921 |
| | Email: usa@opatra.com |
| Contact: | Doris Dong
[Consultant, from Shanghai CV Technology Co., Ltd.]
Add: Room 903, No. 19 Dongbao Road, Songjiang Area, Shanghai, 201613 China
E-mail: doris.d@ceve.org.cn
Tel: 86 21-31261348 / Fax: 86 21-57712250 |
| 2. Device Description | |
| Proprietary Name: | SYNERGY MARBLE |
| Model: | OPASM |
| Classification Name: | Light Based Over The Counter Wrinkle Reduction (OHS)
Over-The-Counter Powered Light Based Laser For Acne (OLP) |
| Regulation Number: | 21 CFR 878.4810 |
| Product Code: | OHS, OLP |
| Device Class: | II |
| Review Panel: | General & Plastic Surgery |
| Device Description: | The SYNERGY MARBLE is an over-the-counter, battery powered
hand-held light emitting diode (LED) device that emits light energy in th
red, blue and amber spectrum for the treatment of wrinkles or mild to
moderate inflammatory acne on the face. The SYNERGY MARBLE
components include an applicator, a charging station and an adaptor.
The treatment surface is applied directly to the skin to ensure consistent
administration of light during each treatment. The device does not contain
any user repairable components. The device is sold as Over the Counter
(OTC). |
| Indications for use: | SYNERGY MARBLE is a hand-held device for over-the counter aesthetic
purposes. The device red light and amber light are intended for the use in
treating wrinkles on the face, and the blue light is intended for the treatment
of the mild to moderate inflammatory acne. |
# 3. Substantial Equivalence Devices Identification
| Predicate Device: | K202055- Looper (Model: ZX-579S)- Heat In A Click LLC |
|-------------------|-------------------------------------------------------|
| Reference Device: | K190443- MMSphere™ - Galactic Beauty, LLC |
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| 4. Substantial Equivalence to Predicate device | |
|------------------------------------------------|--|
|------------------------------------------------|--|
| Parameters | New Device | Predicate Device | Reference Device | Remark |
|----------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------|
| 510(k) number | K220064 | K202055 | K190443 | -- |
| Device name | SYNERGY MARBLE | Looper | MMSphereTM | -- |
| Model | OPASM | ZX-579S | / | -- |
| Owner | YRS GROUP INC | Heat In A Click LLC | Galactic Beauty, LLC | -- |
| Product code | OHS, OLP | OHS, OLP | OHS, OLP | Same |
| Class | II | II | II | Same |
| Indication for use | SYNERGY MARBLE is a hand-held device
for over-the counter aesthetic purposes. The
device red light and amber light are intended
for the use in treating wrinkles on the face,
and the blue light is intended for the treatment
of the mild to moderate inflammatory acne. | Looper (Model: ZX-579S) is a hand-held
device for over-the counter aesthetic
purposes. The Photon mode red light is
intended for the use in treating wrinkles on
the face, and the blue light is intended for the
treatment of the mild to moderate
inflammatory acne. | MMSphereTM Light Therapy Device emits
energy in the red, blue and amber regions of
the spectrum, specifically indicated to treat
wrinkles and/or mild to moderate acne. The
MMSphereTM is designed to be used for 20
minute treatments three to seven times per
week. | Similar |
| Use | Over the Counter | Over the Counter | Over the Counter | Same |
| Anatomical site | Entire Face | Entire Face | Entire Face | Same |
| Type | Hand-held | Hand-held | Handheld and stationary | Same |
| Target Population | Individuals with wrinkles and/or mild to
moderate acne on the face | Individuals with wrinkles and/or mild to
moderate acne on the face | Individuals with wrinkles and/or mild to
moderate acne on the face | Same |
| Irradiance source | LED | LED | LED | Same |
| Visible light LEDs | Yes | Yes | Yes | Same |
| LED Array | 8 LEDs, Over 17cm² | 22 LEDs over 12±10%cm² | Not publicly available | Similar |
| Working Modes and
Wavelengths | Mode 1: Red (625nm±3nm)
Mode 2: Blue (465nm±3nm)
Mode 3: Amber (605nm±3nm) | SONIC Mode: 5 intensity levels
PHOTON Mode (two modes):
Red: 630nm±10nm
Blue: 415±10nm | Red: 625nm
Blue: 465nm
Amber: 605nm | Similar |
| Energy density | Red: 55.3mW/cm²±10% | Red: 55mW/cm²±10% | Red: 2.45mW/cm² | Similar |
| | Blue: 48.2mW/cm²±10%
Amber:38.3mW/cm²±10% | Blue: 48mW/cm²±10% | Blue: 1.33mW/cm²
Amber:Not publicly available | |
| Treatment Time | 3 minutes per target area; 2 treatments per
week for 6 weeks | 3 minutes per target area; 2 treatments per
week for 6 weeks | 20 minutes/day, 120days | Same |
| Power Supply | Lithium battery | Lithium battery | Lithium battery | Same |
| Main material | ABS | ABS Plastic & Stainless Steel | Not publicly available | Similar |
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#### 5. Non-clinical Testing
The SYNERGY MARBLE has been evaluated the safety and performance by lab bench testing and conforms to the following international concensus standards: Electrical safety:
- ANSI AAM ES66601-1: 2005/R)2012 And A1:2012, C1:2009(R)2012 And A.22010(R)2012 (Consolidated Text) Medical Electrical Equipment Patt 1: General . Requirements For Basic Safety And Essential Performance (IEC 60601-1:2005, MOD);
## EMC:
- . IEC 60601-1-2 Edition 4.0 2014-02, Medical equipment - Part 1-2: General requirements for base safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests;
### Additional safety testing:
- IEC 60601-1-6 Edition 3.1 2013-10 Medical electrical equirements for basic satety and essential performance Collateral standard: Usbility; ●
- IEC 60601-1-11 Edition 2.0 2015-01 Medical equipment Part 1-11: General requirements for basic and essential performace Collated Standard: ● Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment;
- IEC 62471 First edition 2006-07 Photobiological safety of lamps and lamp systems;
- IEC 62133-2, Edition1.0 2017-02 Secondary cells and batteries containing alkaline or other non-acid electroytes Safety requirements for portable sealed secondary cells, ● and for batteries made from them, for use in portable applications - Part 2: Lithium systems;
Biocompatibility testing:
- ISO 10993-5:2009/(R) 2014, Biological Evaluation Of Medical Devices -- Part 5: Tests For In Vitro Cytotoxicity. ●
- ISO 10993-10 Third Edition 2010-08-01, Biological Evaluation Of Medical Devices Part 10: Tests For Irritation And Skin Sensitization. ●
- ISO 10993-11 Third edition 2017-09 Biological evaluation of medical devices - Part 11: Tests for systemic toxicity.
### 6. Conclusions
The conclusion drawn from the non-chnical tests dence is as safe, as safe, as effective, and performs as well as the legally marketed predicate device K20205 and reference device K190443.
---
**Source:** [https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OHS/K220064](https://fda.innolitics.com/submissions/SU/subpart-e%E2%80%94surgical-devices/OHS/K220064)
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