Clear Bi-Light

K153081 · Michael Todd, LP · OLP · Feb 15, 2016 · General, Plastic Surgery

Device Facts

• Record ID: K153081
• Device Name: Clear Bi-Light
• Applicant: Michael Todd, LP
• Product Code: OLP · General, Plastic Surgery
• Decision Date: Feb 15, 2016
• Decision: SESE
• Submission Type: Traditional
• Regulation: 21 CFR 878.4810
• Device Class: Class 2
• Attributes: Therapeutic

Intended Use

The Clear Bi-Light is indicated for the treatment of mild to moderate inflammatory acne.

Device Story

Clear Bi-Light is a handheld, over-the-counter LED phototherapy device for treating mild to moderate inflammatory acne. It features interchangeable treatment heads emitting blue light (405-420 nm) and red light (630-660 nm). The device is operated by the patient at home. It includes a contact sensor in the treatment face that activates the LEDs only when pressed against the skin. A microprocessor controls the treatment cycle, which is limited to 3-minute segments per area. The device provides audio signals and indicator lights to guide the user through the treatment process. By applying light therapy to the skin, the device aims to reduce acne inflammation. It is powered by a rechargeable lithium-ion battery.

Clinical Evidence

No clinical data was provided. Substantial equivalence was established through bench testing, including biocompatibility (cytotoxicity, sensitization, irritation per ISO 10993-1), electrical safety (IEC 60601-1), electromagnetic compatibility (IEC 60601-1-2), and photobiological safety (IEC 62471). Software verification and validation were also performed.

Technological Characteristics

Handheld LED phototherapy device; wavelengths: 405-420 nm (blue) and 630-660 nm (red). Materials: Rigid ABS, clear polycarbonate lens cover. Energy source: Rechargeable lithium-ion battery. Connectivity: Standalone. Standards: IEC 60601-1 (safety), IEC 60601-1-2 (EMC), IEC 62471 (photobiological safety), ISO 10993-1 (biocompatibility). Microprocessor-controlled treatment timing.

Indications for Use

Indicated for the treatment of mild to moderate inflammatory acne in patients.

Regulatory Classification

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

• Tanda Mini Skincare System (K124042)
• Silkn Blue (K121435)
• OmniLux Clear U (K081307)

Submission Summary (Full Text)

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Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized symbol of three human profiles facing right, stacked on top of each other, with flowing lines connecting them.

Public Health Service

Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002

February 15, 2016

Michael Todd, LP % Sheila Hemeon-Heyer, JD, RAC Heyer Regulatory Solutions LLC 125 Cherry Lane Amherst, Massachusetts 01002

Re: K153081 Trade/Device Name: Clear Bi-light 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: OLP Dated: January 20, 2016 Received: January 20, 2016

Dear Sheila Hemeon-Heyer:

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. 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.

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

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related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.

If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), please contact the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. 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

http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance.

You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number [phone] or [phone] or at its Internet address

http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm.

Sincerely yours.

## Jennifer R. Stevenson -S

For Binita S. Ashar, M.D., M.B.A., F.A.C.S. Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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## Indications for Use

510(k) Number (if known) K153081

Device Name Clear Bi-Light

Indications for Use (Describe)

The Clear Bi-Light is indicated for the treatment of mild to moderate inflammatory acne.

Type of Use (Select one or both, as applicable)

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

This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of 21 CFR 807.92.

| A. | Submitter: | Heyer Regulatory Solutions, LLC<br>P.O. Box 2151<br>Amherst, MA 01004-2151 |
|----|------------|----------------------------------------------------------------------------|
| | Contact: | Sheila Hemeon-Heyer<br>[e-mail] |

#### Device Manufacturer / 510(k) Applicant B.

| | Michael Todd, LP |
|----------|-------------------------|
| | 648 Port St Lucie Blvd |
| | Port St Lucie, FL 34953 |
| Contact: | Lilia Friend |
| | Senior Vice President |
| Tel: | [phone] |
| Email: | [e-mail] |

#### C. Date Prepared: October 23, 2015

#### Device Name and Classification Information: D.

| Trade Name: | Clear Bi-Light |
|----------------------|--------------------------------------------------------|
| Common/usual Name: | Light Emitting Diode Therapy System |
| Classification Name: | Over-the-Counter Powered Light Based Laser for<br>Acne |
| Product Code, CFR: | OLP, 21 CFR 878.4810 |
| Review Panel: | General and Plastic Surgery Devices |
| Class: | II |

- E. Predicate Device: Tanda Mini Skincare System, K124042 Silkn Blue, K121435 OmniLux Clear U, K081307

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#### Device Description: ட்

The Clear Bi-Light is a hand-held, light emitting device for treating mild to moderate acne. The Clear Bi-Light is non-prescription and is intended for over-the-counter sale. Each Clear Bi-Light package includes the following:

- One Clear Bi-Light rechargeable handpiece ●
- Two Treatment Heads o
- O One blue light (405 - 420 nm)
- One red light (630 660 nm) o
- One Charger Stand ●
- One AC adaptor power cord ●
- One pair goggles
- The Clear Bi-Light Instruction Manual

Image /page/4/Figure/12 description: The image shows a Michael Todd Clear BIIGHT device with its charger stand. The device has a treatment head with LEDs covered by clear polycarbonate, which is referred to as the treatment head face. The device also has a power on/off button with an indicator light, a treatment head release lever, and a DC input for charging.

## F. Indication for Use:

The Clear Bi-Light is indicated for the treatment of mild to moderate inflammatory acne.

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Section 8: 510(k) Summa

## Technical Comparison with Predicate Devices க்

nformation for predicate devices was obtained from publicly available sources, including the 510(k) Summaries and device
nstruction manuals.

| | Indication for Use | OTC or Rx? | Energy source | Treatment heads | Wavelength(s) (nm) | Comparison | | Clear Bi-Light | Tanda Mini*<br>K124042 | Silkn Blue<br>K121435 | OmniLux Clear U<br>K081307 | Comparison |
|-------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------|------------|---------------|---------------------------------------------------------|----------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------|
| Clear Bi-Light | Indicated for the treatment of mild to moderate inflammatory acne. | OTC | LED | Separate Blue and Red, treatment heads | 405-420<br>630-660 | | Treatment<br>control(s) | On/off button puts<br>device in standby<br>mode<br>Contact sensor in<br>treatment face,<br>touching device to<br>face activates LEDs | On/off button puts<br>device in standby<br>mode<br>Contact sensor in<br>treatment face,<br>touching device to<br>face activates LEDs | On/off button | Three position<br>switch: Off - Blue<br>- Red | All devices have<br>on/off button.<br>Contact sensor in<br>proposed device is<br>the same as in the<br>Tanda Mini. |
| Tanda Mini* K124042 | Generally indicated to treat dermatological conditions. Specifically, Blue light modules are indicated to treat mild to moderate inflammatory acne. | OTC | LED | Blue only | $414 \pm 6$ | | Treatment<br>indicator(s) | Indicator light - Solid<br>green while<br>treatment is in<br>process; blinking<br>indicates low battery.<br>Audio signal: long<br>beep when power is<br>turned on, short beep<br>every 30 seconds<br>during treatment;<br>long beep at end of 3<br>minute cycle | Indicator light -<br>flashing green when<br>treatment is being<br>delivered<br>Audio signal: one<br>beep every 30<br>seconds during<br>treatment; 2 beeps<br>at end of treatment<br>or low battery; 3<br>beeps signals high<br>temperature on<br>treatment head; 4<br>beeps signals<br>treatment head is<br>disconnected. | Indicator light -<br>Solid green when<br>ready for treatment<br>or battery fully<br>charged; blinking<br>green for low<br>battery; orange for<br>battery charging; | None | Indicator light<br>substantially<br>equivalent to Tanda<br>Mini and Silkn Blue.<br>Audio signal<br>substantially<br>equivalent to Tanda<br>Mini |
| Silkn Blue K121435 | Indicated as an over the counter phototherapy device for the treatment of mild to moderate acne. | OTC | LED | Blue only | $415 \pm 15$ | Same | Treatment<br>timer | Yes<br>Up to 3 minute<br>treatment per area<br>after which device<br>returns to standby<br>mode. Must press<br>treatment face<br>against skin to<br>reactivate lights | Yes<br>Up to 3 minute<br>treatment per area<br>after which device<br>turns off. Must<br>press power button<br>to reactivate. | No | No | Substantially<br>equivalent to Tanda<br>Mini. Both devices<br>limit each treatment<br>to 3 minute<br>segments. |
| OmniLux Clear U K081307 | Indicated to treat mild to moderate acne on the face. | OTC | LED | Blue and Red in same head, chosen using selector switch | $415 \pm 5$<br>$633 \pm 6$ | Substantially equivalent. Minor wording differences do not change indication for use. | | | | | | |
| | | | | | | Same as OmniLux (both offer separate blue and red light treatments). All devices offer blue light treatments. Substantially equivalent. Wavelengths are in the blue and red spectrum. | | | | | | |

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# Section 8: 510(k) Summar

Michael Todd, LP
Clear Bi-Light 510(k)

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| Treatment<br>regimen | Clear Bi-Light | Tanda Mini*<br>K124042 | Silkn Blue<br>K121435 | OmniLux Clear U<br>K081307 | Comparison |
|--------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------|
| Dose rate<br>(mW/cm²) | 31.1 (blue)<br>54.6 (red) | 22.4 | 50 | 40 (blue)<br>70 (red) | Substantially equivalent. Proposed treatment regimen is essentially the same as for Tanda Mini and Silkn Blue |
| Treatment face<br>area (cm²) | 20 | 27 | 7 | 28.7 | Substantially equivalent - within dose rate ranges of predicate devices |
| Max treatment<br>temperature<br>(°C) | 38°C (blue)<br>40°C (red) | 39-43 | 41 ± 2 | 39-43 | Substantially equivalent - within size ranges of predicate devices |
| Microprocessor<br>controlled | Yes | Yes | Yes | Unknown | Substantially equivalent - within temperature ranges of predicate devices |
| Handheld | Yes | Yes | Yes | Yes | Same |
| Patient<br>contacting<br>materials | Rigid ABS<br>Clear polycarbonate<br>lens cover | Rigid ABS | Stainless steel<br>Rigid ABS | Rigid ABS | Substantially equivalent.<br>Biocompatibility compliant with ISO 10993. |
| Treatment<br>regimen | Hold treatment face<br>in contact with skin.<br>Apply blue light for<br>up to 3 minutes per<br>skin area, followed<br>by red light for up to<br>3 minutes per skin<br>area. Can be used<br>daily. | Hold treatment face<br>in contact with skin<br>and apply blue light<br>for up to 3 minutes<br>per skin area. Can<br>be used daily | Hold treatment face<br>in contact with skin<br>for 3 to 4 minutes,<br>then move to<br>another area. Can<br>be used daily. | Alternate<br>treatments of blue<br>and red light twice<br>a week for 20<br>minutes per<br>treatment | Same |
| | Clear Bi-Light | Tanda Mini*<br>K124042 | Silkn Blue<br>K121435 | OmniLux Clear U<br>K081307 | Comparison |
| Power supply | Lithium-ion rechargeable battery<br>AC charger: 100-240V at 50-60Hz, 500 mA | NiMH rechargeable battery or AC power supply<br>AC charger: 100-240V, 50-60 Hz, 400 mA | Lithium-ion rechargeable battery<br>AC charger: 100-240V, 50-60 Hz, 400 mA | "A separate, universal, power supply converts mains AC power to the DC power required" | Same as Silkn Blue |
| Dimensions | 6.4 cm x 3.5 cm x 14.6 cm<br>(2.5 in x 1.4 in x 5.7 in) | 6.4 cm x 5.6 cm x 12.2 cm<br>(2.5 in x 2.2 in x 4.8 in) | 7.5 cm x 5 cm x 16.4 cm<br>(3 in x 2 in x 6.5 in) | 6 cm x 4 cm x 12 cm<br>(2.4 in x 1.6 in x 4.7 in) | Substantially equivalent. All are small, hand-held devices. |
| Weight | 107.1 g (6 oz) | 340.2 g (12 oz) | 231 g (8.1 oz) | Unknown | Substantially equivalent. All are light-weight, hand-held devices. |

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# ection 8: 510(k) Summa

There are e indication for use of the Clear Bi-Light device is the same as the technical specification
the Clear Bi-Light device are either the same or substantially equivaled the pred

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## H. Nonclinical Testing

The following nonclinical testing was provided in this 510(k):

Biocompatibility Testing - The skin contacting material of the device (hydrogel) was subjected to biocompatibility testing per ISO 10993-1:2009, "Biological Evaluation of Medical Devices – Part 1: Evaluation and Testing," for devices in contact with intact skin, including cytotoxicity, dermal sensitization, and dermal irritation. All tests passed.

Electrical Safety and Electromagnetic Compatibility Testing - The Clear Bi-Light has been tested and complies with the applicable requirements of the following standards for medical devices used in the home environment:

- . IEC 60601-1:2005 Medical Electrical Equipment - Part 1: General Requirements for Safety, 3rd edition
- IEC 60601-1-2:2007 Medical electrical equipment Part 1-2: General . requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests, 300 edition

Photobiological Safety Testing - The Clear Bi-Light has been tested and complies with IEC 62471:2006-07, Photobiological safety of lamps and lamp systems, 186 edition. This IEC standard incorporates the principles of the following ANSI IESNA recommended practices:

- o RP 27.1:2005 Recommended practice for photobiological safety for lamps and lamp systems - General requirements
- RP 27.2:2000 Recommended practice for photobiological safety for lamps and lamp systems - Measurement techniques
- RP-27.3:2007 Recommended practice for photobiological safety for lamps ● and lamp systems - Risk group classification and labeling

Software Verification and Validation - Software documentation consistent with moderate level of concern was submitted in this 510(k). System validation testing presented in this 510(k) demonstrated that all software requirement specifications are met and all software hazards have been mitigated to acceptable risk levels.

## I. Conclusions

The information and testing presented in this 510(k) demonstrates that the Clear Bi-Light performs as designed and intended and is substantially equivalent for the treatment of mild to moderate inflammatory acne.