EON
Device Facts
| Record ID | K211681 |
|---|---|
| Device Name | EON |
| Applicant | Dominion Aesthetic Technologies, Inc. |
| Product Code | PKT · General, Plastic Surgery |
| Decision Date | Mar 30, 2022 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 878.5400 |
| Device Class | Class 2 |
| Attributes | Therapeutic |
Indications for Use
The EON (1064nm laser) is intended for non-invasive lipolysis of the abdomen and flanks to achieve disruption of adipocyte cells intended for non-invasive aesthetic use to achieve a desired aesthetic effect. It is intended for individuals with a Body Mass Index of 30 or less.
Device Story
EON is a 1064nm diode laser system for non-invasive lipolysis of abdomen and flanks. Operated by clinicians in a clinic setting, the device uses a robotic arm to position a non-contact treatment head over the target area. The system delivers concurrent 1064nm laser energy and jet impingement cooling air. The laser heats adipose tissue to 42°C–50°C to induce adipocyte apoptosis, while the cooling system maintains skin temperature below 43°C. The device monitors skin temperature in real-time and automatically terminates laser emission if the temperature exceeds 43°C. By reducing subcutaneous adipose tissue, the device improves the appearance of visible fat bulges, providing aesthetic benefits to patients. The system operates on 110V power.
Clinical Evidence
Prospective clinical study evaluated safety and efficacy for flank fat reduction. 33 subjects treated for 20 minutes. Primary endpoint: blinded photo evaluation (success defined as 2 of 3 readers correctly identifying ≥9 of 11 pre/post sets). Results: 81.8% (27/33) sets correctly scored; study success achieved. Secondary endpoints: mean subcutaneous adipose thickness reduction of 6.1 mm per flank (12.1 mm per patient, -15%, p<0.01) at 12 weeks. Mean pain score 1.95/10 during procedure. One adverse event (palpable thickening) resolved by 12 weeks. 100% subject satisfaction.
Technological Characteristics
1064nm diode laser; continuous wave mode; 1-20s pulse length; max power density 1.4 W/cm². Non-contact delivery via articulated robotic arm. Jet impingement cooling system. 110V supply voltage. Standards: IEC 60601-1 (electrical safety), IEC 60601-1-2 (EMC), IEC 60601-2-22 (laser safety), IEC 60825-1 (laser classification).
Indications for Use
Indicated for non-invasive lipolysis of abdomen and flanks in individuals with BMI ≤ 30 to disrupt adipocyte cells for aesthetic fat reduction.
Regulatory Classification
Identification
A Low Level Laser System for Aesthetic Use is a device using low level laser energy for the disruption of adipocyte cells within the fat layer for the release of fat and lipids from these cells for noninvasive aesthetic use.
Special Controls
*Classification.* Class II (special controls). The special control for this device is the FDA guidance document entitled “Guidance for Industry and Food and Drug Administration Staff; Class II Special Controls Guidance Document: Low Level Laser System for Aesthetic Use.” See § 878.1(e) for the availability of this guidance document.
Predicate Devices
- Sculpsure (K160470)
Submission Summary (Full Text)
{0}------------------------------------------------
Image /page/0/Picture/0 description: The image contains the logos of the Department of Health & Human Services and the Food and Drug Administration (FDA). The Department of Health & Human Services logo is on the left, and the FDA logo is on the right. The FDA logo includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG" in blue and "ADMINISTRATION" in a smaller font size below.
Dominion Aesthetic Technologies, Inc. Ahmed Mohammed VP, Product Development 2431 Aloma Avenue Suite 225 Winter Park, Florida 32792
August 11, 2022
Re: K211681 Trade/Device Name: EON Regulation Number: 21 CFR 878.5400 Regulation Name: Low level laser system for aesthetic use Regulatory Class: Class II Product Code: PKT
Dear Ahmed Mohammed:
The Food and Drug Administration (FDA) is sending this letter to notify you of an administrative change related to your previous substantial equivalence (SE) determination letter dated March 30, 2022. Specifically, FDA is updating this SE Letter to remove OOK and GEX as an administrative correction. because OOK (Dermal Cooling Pack/Vacuum/Massager) and GEX (Powered Laser Surgical Instrument) do not apply to your device.
Please note that the 510(k) submission was not re-reviewed. For questions regarding this letter please contact Long Chen, Ph.D., OHT4: Office of Surgical and Infection Control Devices, 301-796-6389, Long.Chen@fda.hhs.gov.
Sincerely,
Long H. Chen -S Digitally signed by Long H. Chen -S
Date: 2022.08.11 13:57:54 -04'00'
Long Chen, Ph.D. Director (Acting) DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
{1}------------------------------------------------
Image /page/1/Picture/0 description: The image contains two logos. On the left is the Department of Health and Human Services logo. On the right is the FDA logo, which includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text.
March 30, 2022
Dominion Aesthetic Technologies, Inc. Ahmed Mohammed VP, Product Development 2431 Aloma Avenue Suite 225 Winter Park, Florida 32792
Re: K211681
Trade/Device Name: EON 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: GEX, OOK, PKT Dated: February 28, 2022 Received: February 28, 2022
Dear Ahmed Mohammed:
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.
{2}------------------------------------------------
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 and Part 809); 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 medical devices and radiation-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,
## Purva U. Pandya -S
Purva Pandya, D.Eng. Assistant Director DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
{3}------------------------------------------------
## Indications for Use
510(k) Number (if known) K211681
Device Name EON
Indications for Use (Describe)
The EON (1064nm laser) is intended for non-invasive lipolysis of the abdomen and flanks to achieve disruption of adipocyte cells intended for non-invasive aesthetic use to achieve a desired aesthetic effect. It is intended for individuals with a Body Mass Index of 30 or less.
Type of Use (Select one or both, as applicable)
| <span style="font-size: 10pt;"> <span style="font-family: Symbol;">☑</span> Prescription Use (Part 21 CFR 801 Subpart D)</span> |
|---------------------------------------------------------------------------------------------------------------------------------|
| <span style="font-size: 10pt;"> <span style="font-family: Symbol;">☐</span> Over-The-Counter Use (21 CFR 801 Subpart C)</span> |
_ Over-The-Counter Use (21 CFR 801 Subpart C)
## CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
### *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
> Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
{4}------------------------------------------------
## Section 5: 510(k) Summary
## Table Of Contents
D
| Section 5: 510(k) Summary | 5-1 |
|-----------------------------------------------------------------------------------|------|
| 5-1 Submitter | 5-2 |
| 5-2 Device Information. | 5-2 |
| 5-3 Predicate Device. | 5-3 |
| 5-4 Device Description... | 5-3 |
| 5-5 Indications for Use... | 5-3 |
| 5-6 Comparison of Technological Characteristics with the Predicate Device | 5-4 |
| 5-7 Performance Data | 5-7 |
| 5.7.1 Electrical Safety and Electromagnetic Compatibility (EMC) Testing Conducted | 5-7 |
| 5.7.2 Software Validation & Verification | 5-7 |
| 5.7.3 Other Non-Clinical Testing Conducted. | 5-7 |
| 5.7.4 Summary of the Clinical Study Conducted | 5-8 |
| 5-8 Conclusions | 5-10 |
{5}------------------------------------------------
## 5-1 Submitter
Dominion Aesthetic Technologies, Inc. 2431 Aloma Avenue Suite # 300 Winter Park, FL 32792
Contact Person: Ahmed Mohammed Phone: 763-439-4602 Email: amohammed@dominionaethetic.com
Date Prepared: March 15, 2022
## 5-2 Device Information
Name of Device: EON. Common or Usual Name: Aesthetic Laser System Classification Name: Laser Surgical Instrument For Use In General And Plastic Surgery And In Dermatology (21 CFR 878.4810) Regulatory Class: II Product Code: GEX, OOK and PKT
{6}------------------------------------------------
## 5-3 Predicate Device
Cynosure, Inc., Sculpsure, K160470
## 5-4 Device Description
EON aesthetic laser system is 1064nm diode laser device that is intended for non-invasive lipolysis of the abdomen and flanks in individuals with a Body Mass Index (BMI) of 30 or less. This wavelength is used to affect the appearance of visible fat bulges in the abdomen and flanks.
Both laser energy and cooling air are delivered concurrently through the same treatment head that is positioned by a robotic arm. The treatment head is never in contact with the skin.
During treatment, the desired area will be defined by the physician and will be treated with the 1064nm laser over a 20-minute timeframe. The mechanism of action is to preferentially heat the adipose tissue to temperatures that will induce apoptosis (42°C to 50°C). The cooling system will maintain the skin at comfortable temperature (<43°C).
## 5-5 Indications for Use
The EON (1064nm laser) is intended for non-invasive lipolysis of the abdomen and flanks to achieve disruption of adipocyte cells intended for non-invasive aesthetic use to achieve a desired aesthetic effect. It is intended for individuals with a Body Mass Index of 30 or less.
{7}------------------------------------------------
K211681
# 5-6 Comparison of Technological Characteristics with the Predicate Device
| Parameter | Dominion<br>EON | Cynosure, Inc.<br>SculpSure | Comparison |
|---------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Indications for Use (IFU) | The EON (1064nm laser) is<br>intended for non-invasive<br>lipolysis of the abdomen and<br>flanks to achieve disruption<br>of adipocyte cells intended<br>for non-invasive aesthetic<br>use to achieve a desired<br>aesthetic effect. It is<br>intended for individuals with<br>a Body Mass Index of 30 or<br>less. | Cynosure SculpSure is a<br>diode laser system intended<br>for non-invasive lipolysis of<br>the abdomen and flanks in<br>individuals with a Body Mass<br>Index (BMI) of 30 or less. The<br>device is intended to affect<br>the appearance of visible fat<br>bulges in the abdomen and<br>flanks. | Similar |
| K Number | K211681 | K160470 | N/A |
| Lipolysis Method | Heat-assisted | Heat-assisted | Same |
| Laser Type | Diode | Diode | Same |
| Wavelength | 1064 nm | 1064 nm | Same |
| Power Mode | Continuous Wave (CW) | Continuous Wave (CW) | Same |
| Pulse Length | 1 to 20s | 1 to 20s | Same |
| Parameter | Dominion<br>EON | Cynosure, Inc.<br>SculpSure | Comparison |
| Applicator Size | 75 cm², 110 cm², 150 cm² | 24 cm² (4X) | Similar |
| Application Method | Articulated Scanning Arm, Non-contacting | Belt | Different: EON uses an articulated scanning arm to continuously move the laser beam over the treatment area and, simultaneously, provide skin cooling. EON is similar to SculpSure in principal of operation where both devices deliver laser energy and cool down the skin in the treated area. To ensure safety, EON monitors skin temperature and turn off the laser if the skin temperature exceeds 43°C. EON uses jet impingement cooling (which is more effective than contact cooling), this ensures that the skin in the treated area is safe and comfortable while the laser energy is heating the subcutaneous adipose tissue. EON is as safe, and as effective as SculpSure. |
| Treatment Area | Abdomen and Flanks | Abdomen and Flanks | Same |
| Maximum Power Density | Up to 1.4 W/cm² | Up to 1.4 W/cm² | Same |
| Parameter | Dominion<br>EON | Cynosure, Inc.<br>SculpSure | Comparison |
| Supply Voltage | 110 V; Single Phase | 220 V; Single Phase | Different: EON uses 110V supply voltage to<br>improve usability since 110V is the standard<br>supply voltage the United States. Supply voltage<br>doesn't affect efficacy. EON design meets all<br>applicable electrical safety standards. |
| Supply Current | 20A | 20A | Same |
| Laser Cooling | Closed cycle, internal | Closed cycle, internal | Same |
{8}------------------------------------------------
K211681
-
{9}------------------------------------------------
# I
# DN Premarket Notification 510(k)
{10}------------------------------------------------
## 5-7 Performance Data
## 5.7.1 Electrical Safety and Electromagnetic Compatibility (EMC) Testing Conducted
- . IEC 60601-1-2 Edition 4.0 2014-02 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance
- IEC 60601-1 :2005 (Third Edition) + CORR. 1 :2006 + CORR. 2:2007 +A1 :2012 Medical Electrical Equipment - Part 1: General Requirements for Basic Safety and Essential Performance (IEC 60601-1: 2012 reprint) including compliance with US National Differences demonstrating conformance to the FDA-recognized standard for electrical safety (AAMI/ANSI ES60601-1:2005(R) 2012).
## 5.7.2 Software Validation & Verification
Software verification and validation testing were conducted and documentation was provided as recommended by FDA's Guidance for Industry and FDA Staff, "Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices." The software for this device was considered as a "Moderate" level of concern, since a failure or latent design flaw could directly result in minor injury to the patient or operator.
## 5.7.3 Other Non-Clinical Testing Conducted
- IEC 60601-2-22 Edition 3.1 2012-10 Medical Electrical Equipment Part 2-22: Particular ● Requirements for Basic Safety and Essential Performance of Surgical, Cosmetic, Therapeutic and Diagnostic Laser Equipment
- IEC 60825-1 :2014 (Third Edition) Safety of Laser Products Part 1: Equipment . Classification and Requirements
{11}------------------------------------------------
## 5.7.4 Summary of the Clinical Study Conducted
## 5.7.4.1 Objectives
The primary objective of this study was to confirm the safety of a1064-nm laser device with a novel robotic arm for noninvasive subcutaneous fat reduction in the flank area. Secondary objectives included assessing the extent of subject discomfort during treatment, overall subject satisfaction with the results of the procedure, and a determination of subcutaneous fat reduction in the treated area.
## 5.7.4.2 Efficacy Endpoints
Primary efficacy endpoint: blinded evaluation of pre- and post-treatment photos Secondary efficacy endpoints: mean fat reduction by ultrasound and subject satisfaction.
## 5.7.4.3 Materials and Methods
A 110-cm² area on both flanks of enrolled subjects was treated for 20 minutes with an FDAcleared robotic non-contact 1064-nm laser system (EON®; Dominion Aesthetic Technologies, Inc.). Patients were followed for 12 weeks, and examined routinely at 2 weeks, 12 weeks and additionally as needed, post-treatment. Pre- and post-treatment photos were taken by a professional photographer using a standardized DSLR and lighting set-up. The ability of three independent readers to correctly identify blinded pre-treatment vs. post-treatment photos was assessed. The study was declared to be a success if at least two of the three independent readers correctly identified at least 9 of the 11 photos as pre-treatment. Ad hoc surveys were administered to assess patient satisfaction. A 2-week post-treatment ultrasound scan was used to check for changes in the treated area. The study was powered to assess patient-level and flank-level subcutaneous adipose tissue thickness using ultrasound measurements taken at a center of each treatment zone prior to treatment and at 12 weeks post-treatment for efficacy determination, with mean thicknesses calculated per subject and per flank.
## 5.7.4.4 Results
The treatment had a low incidence of adverse effects, with only one subject developing a palpable thickening in the subcutaneous tissue following treatment. This was noted at the two-week time period and had resolved by the 12-week post-treatment exam. No other predefined adverse effects were noted. On a scale of 0 to 10, the mean pain score during the procedure was 1.95, decreasing to 0.9 at 30 minutes post-procedure. Subject satisfaction was "Excellent" for all subjects (100%). For blinded evaluation of pre- and post-treatment photos, 27 (81.8%) of 33 image sets were correctly scored overall, with two of the three readers correctly identifying pre- and post-treatment photos in at least 9 of the 11 subjects, thus achieving study success. At Week 12 after one treatment, the mean reduction in
{12}------------------------------------------------
subcutaneous adipose thickness on the treated flanks was 6.1 mm per flank and 12.1 mm per patient (-15%; p<0.01, both measures).
Similar to the prior abdominal study with the same robotic laser device, this study confirms the safety of this 1064-nm non-contact laser device for treating subcutaneous fat on the flanks. The study provided objective evidence of EON safety and efficacy in treating the flank area.
{13}------------------------------------------------
## 5-8 Conclusions
D
The clinical and non-clinical testing conducted on EON support the safety of the device and the hardware and software verification and validation demonstrate that EON should perform as intended in the specified use conditions. Dominion believes that EON is as safe, as effective, and performs as well as the predicate device. The clinical performance of EON demonstrates that EON has a safety and effectiveness profile that is similar to its predicate device. It has been concluded that the EON device is safe and effective for its intended use.
