Who is the manufacturer of Delight, Delight ortho, B&Lite S?

Dentall Co., Ltd. filed the 510(k) submission for Delight, Delight ortho, B&Lite S (K170529).

What is the FDA product code for Delight, Delight ortho, B&Lite S?

EBZ. It is classified under 21 CFR 872.6070 as a Class 2 device in the Dental panel.

What is the regulatory pathway for Delight, Delight ortho, B&Lite S?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like Delight, Delight ortho, B&Lite S?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Delight, Delight ortho, B&Lite S

Q: What are the predicate devices for Delight, Delight ortho, B&Lite S?

Hi-Light, Hi-Light plus (K140432).

K170529 · Dentall Co., Ltd. · EBZ · Aug 8, 2017 · Dental

Device Facts

Record ID	K170529
Device Name	Delight, Delight ortho, B&Lite S
Applicant	Dentall Co., Ltd.
Product Code	EBZ · Dental
Decision Date	Aug 8, 2017
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 872.6070
Device Class	Class 2
Attributes	Therapeutic

Intended Use

For light curing polymerization of dental composites, luting materials, cements and other light cured materials

Device Story

Delight, Delight ortho, and B&Lite S are cordless, LED-based dental curing lights; used by dental professionals to polymerize light-cure resin-based composites, luting materials, and cements. Devices emit narrow-spectrum blue light (430-490nm) to activate CPQ molecules in dental monomers. Handheld, battery-operated design ensures portability. To prevent cross-contamination, devices are used with FDA-cleared disposable barrier sheaths (TIDIShield). Clinicians select specific operation modes (Standard, High/Fast, Soft Start, Pulse/Sequential, Ortho/Turbo) based on required light intensity and duration to achieve optimal polymerization. Output intensity ranges from 800 to 2,700 mW/cm² depending on the model and mode. Benefits include efficient, portable, and controlled light-curing for various dental restorative procedures.

Clinical Evidence

Bench testing only. Performance evaluated via optical power testing, spectral irradiance (wavelength spectrum), and depth of cure (composite hardness testing) in accordance with ANSI/ADA Specification No. 48:2004, ANSI/ADA Specification No. 48-2:2010, and FDA guidance for dental curing lights. Electrical safety and EMC testing performed per IEC 60601-1:2005+A1:2012 and IEC 60601-1-2:2007. All results conformed to standards.

Technological Characteristics

LED-based dental curing light; 10W LED source; 430-490nm wavelength (460nm peak). Powered by internal 3.7Vdc 2200mAh Li-ion battery; rechargeable via AC/DC adapter (100-240Vac). Handheld form factor. Patient contact via disposable barrier sheath. Compliance: IEC 60601-1, IEC 60601-1-2, ANSI/ADA Specification No. 48, ANSI/ADA Standard No. 48-2.

Indications for Use

Indicated for light curing polymerization of dental composites, luting materials, cements and other light cured materials in a dental clinical setting.

Regulatory Classification

Identification

An ultraviolet activator for polymerization is a device that produces ultraviolet radiation intended to polymerize (set) resinous dental pit and fissure sealants or restorative materials by transmission of light through a rod.

Predicate Devices

Hi-Light, Hi-Light plus (K140432)

Reference Devices

TIDIShield Curing Light Sheath (K132953)

Related Devices

K140432 — HI-LIGHT, HI-LIGHT PLUS · Dentall Corporation · Aug 3, 2015
K153514 — Premium Plus C01/C02 LED Curing Light · Premium Plus International Limited · Aug 22, 2016
K051571 — SKYLIGHT LED CURING LIGHT · Dmetec.Co., Ltd. · Jul 19, 2005
K173876 — Cybird LED Curing Light · Dxm Co., Ltd. · Jan 24, 2018
K080025 — LED.L, LED.M, LED.G, LED.B · Guilin Woodpecker Medical Instrument Co., Ltd. · Mar 19, 2008

Submission Summary (Full Text)

{0}------------------------------------------------ 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 an abstract symbol that resembles an eagle or a stylized human profile, composed of three overlapping shapes. Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 DENTALL Co., Ltd c/o DongHa Lee KMC, Inc. Room no., 904, 27, Digital-ro 27ga-gil, Guro-gu Seoul 08375 KOREA August 8, 2017 Re: K170529 Trade/Device Name: Delight, Delight Ortho, B&Lite S Regulation Number: 21 CFR 872.6070 Regulation Name: Ultraviolet activator for polymerization Regulatory Class: Class II Product Code: EBZ Dated: June 23, 2017 Received: July 5, 2017 #### Dear DongHa Lee: 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. Isting 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. {1}------------------------------------------------ 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 (reporting of medical device-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 (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/Resourcesfor You/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR 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 (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Sincerely, Mary S. Runner -S Michael Ryan Acting Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # Change Control Table, Change History # Change Control Table | Version | Document Author | Document Approver | Date Approved | |---------|---------------------|---------------------|---------------| | 1.00 | Name, Title, Office | Name, Title, Office | MM/DD/YYYY | Complete Change Control Table (all versions) retained in SWIFT Docs. {3}------------------------------------------------ # Indications for Use 510(k) Number (if known) K170529 Device Name Delight, Delight ortho, B&Lite S Indications for Use (Describe) For light curing polymerization of dental composites, luting materials, cements and other light cured materials | Type of Use (Select one or both, as applicable) | | |-------------------------------------------------|--| |-------------------------------------------------|--| |X Prescription Use (Part 21 CFR 801 Subpart D) | | 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}------------------------------------------------ Image /page/4/Picture/0 description: The image shows the logo for "Dentalall". The word "Dental" is written in bold, black letters, with a light purple swoosh above it. The "all" portion of the logo is in white letters inside of a green parallelogram. # 510(k) Summary (K170529) Date: August 9, 2017 # 1. Applicant / Submitter DENTALL Co., Ltd. Address: 301-905, Bucheontechnopark, 345, Seokcheon-ro, Ojeong-gu, Bucheon-si, Gyeonggi-do, 14501, Korea Tel: +82-32-327-6026 Fax: +82-32-327-6027 Establishment registration number: 3009307635 ## 2. Submission Contact Person DongHa Lee (Consultant / KMC, Inc.) Address: Room no. 904, 27, Digital-ro 27ga-gil, Guro-gu, Seoul, 08375, Korea Tel: +82-70-8965-5554 Fax: +82-2-2672-0579 Email: dhlee@kmcerti.com ## 3. Device Information - · Trade Name: Delight, Delight ortho, B&Lite S - Common Name: Dental curing light - Device Classification: Class II - Classification Name: Ultraviolet activator for polymerization . - Product Code: EBZ - Classification regulation: 21CFR 872.6070 ## 4. Predicate Device - · Hi-Light, Hi-Light plus (K140432) by DENTALL Co., Ltd. ## 5. Device Description Delight, Delight ortho and B&Lite S are light-emitting diode (LED) type dental curing light that is {5}------------------------------------------------ Image /page/5/Picture/0 description: The image shows the logo for "Dentall". The word "Dentall" is written in a bold, sans-serif font. The "Dent" part of the word is in black, while the "all" part is in white against a green parallelogram. There is a light purple swoosh design to the left of the word. used for polymerization of light cure resin based composites. They can be used on several different dental materials that are curable by light. The devices use LED that produce a narrow spectrum of blue light in the 430~490nm range, which is useful energy range for activating the CPQ molecule, most commonly used to initiate the photo polymerization of dental monomers. The devices are designed by considering lightweight and portability. They operate on a rechargeable battery, making it easier to carry and use. The device is not provided sterile and is not intended to be sterilized when used. To prevent cross contamination, users must cover the device with FDA cleared barrier sheath (K132953/ TIDIShield™ Curing Light Sheath). It should be changed between each patient. ## 6. Indication for use For light curing polymerization of dental composites, luting materials, cements and other light cured materials. # 7. Substantial Equivalence Delight, Delight ortho and B&Lite S are substantially equivalent to the predicate devices, Hi-Light, Hi-Light plus (K140432) by DENTALL Co., Ltd. in terms of intended use, technology and principle of operation. The following comparison table is presented to demonstrate substantial equivalence. | Descriptive Information | Subject Device | | | Predicate Device | | |----------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Device Name | Delight | Delight ortho | B&Lite S | Hi-Light | Hi-Light plus | | Manufacturer | DENTALL Co., Ltd. | | | DENTALL Co., Ltd. | | | 510(k) number | - | | | K140432 | | | Product Code | EBZ | | | EBZ | EBZ | | Regulatory Class | 2 | | | 2 | | | Indications for use | For light curing polymerization of dental composites, luting materials, cements and other light cured materials. | | | For light curing polymerization of dental composites, luting materials, cements and other light cured materials. | | | Device Design - Operation Mode (Standard / Normal Power Mode) | 1) Optical output: 1,200 $mW/cm² (±10%)$ 2) Available time setting: 5, 10, 15, 20 seconds | 1) Optical output: 1,200 $mW/cm² (±10%)$ 2) Available time setting: 5, 10, 15, 20 seconds | 1) Optical output: 800 $mW/cm² (±10%)$ 2) Available time setting: 5, 10, 15, 20 seconds | 1) Optical output: 700 $mW/cm² (±10%)$ 2) Available time setting: 10, 15, 20, 30 seconds | 1) Optical output: 1,000 $mW/cm² (±10%)$ 2) Available time setting: 5, 10, 15, 20 seconds | | Device Design - Operation Mode (High / Fast Power | 1) Optical output: 1,800 $mW/cm² (±10%)$ 2) Available time | 1) Optical output: 2,700 $mW/cm² (±10%)$ 2) Available time | 1) Optical output: 1,200 $mW/cm² (±10%)$ 2) Available time | 1) Optical output: 1,400 $mW/cm² (±10%)$ 2) Available time | 1) Optical output: 1,600 $mW/cm² (±10%)$ 2) Available time | | Mode) | setting: 3, 6, 9, 12 seconds | setting: 2, 3, 5, 10 seconds | setting: 3, 6, 9, 12 seconds | setting: 5, 10, 15, 20 seconds | setting: 3, 5, 10, 15 seconds | | Device Design - Operation Mode (Soft Start Mode) | 1) Optical output: After gradually increasing from 0 to 1,800 mW/cm²(±10%) and be maintained until finish time 2) Available time setting: 5, 10, 15 seconds | | 1) Optical output: After gradually increasing from 0 to 1,200 mW/cm²(±10%) and be maintained until finish time 2) Available time setting: 5, 10, 15 seconds | 1) Optical output: After gradually increasing from 0 to 2,000 W/cm² (±10%) and be maintained until finish time 2) Available time setting: 10, 15, 20 seconds | 1) Optical output: After gradually increasing from 0 to 1,600 mW/cm² (±10%) and be maintained until finish time 2) Available time setting: 5, 10, 15 seconds | | Device Design - Operation Mode (Pulse / Sequential Power Mode) | 1) Optical output: Repeat 0 and 1,800 mW/cm² (±10%) continuously 2) Available time setting: 10, 15, 20 seconds | 1) Optical output: 2,700 mW/cm² (±10%). Repeat it 8 times at intervals of 2 second. 2) Available time setting: 2, 3, 4, 5 seconds | | 1) Optical output: Repeat 0 and 2,000 mW/cm² (±10%) continuously 2) Available time setting: 10, 15, 20 seconds | 1) Optical output: 2,700 mW/cm² (±10%). Repeat it 8 times at intervals of 2 second. 2) Available time setting: 1, 2, 3, 4 seconds | | Device Design - Operation Mode (General Orthodontic / Turbo Mode) | | | 1) Optical output: 1,800 mW/cm²(±10%) 2) Available time setting: 2, 4, 6 seconds | 1) Optical output: 2,000 mW/cm² (±10%) 2) Available time setting: 3, 5, 10, 15 seconds | | | Device Design - Operation Mode (Fast Orthodontic / Extra Mode) | | | 1) Optical output: 2,700 mW/cm²(±10%) 2) Available time setting: 1, 2, 3 seconds | | 1) Optical output: 3,000 mW/cm² (±10%) 2) Available time setting: 1, 2, 3, 4 seconds | | Device Design - Light source | 10W LED | | | 10W LED | | | Device Design - Power source of handpiece | Rechargeable Li-ion battery (3.7Vdc. 2200mAh) | | | Rechargeable Li-ion battery (3.7Vdc) | | | Device Design - Power source of battery charger | AC/DC Adapter (Input: 100-240Vac, 50/60 Hz, 400 mA Output: 5.0Vdc, 1.6A) | | | AC/DC Adapter (Input: 100-240Vac, 50/60 Hz, 400 mA Output: 5.0Vdc) | | | Device Design - Accessories | Handpiece , Battery charger, Battery pack, Anti- glare shield, Light guide, AC/DC adapter | | | Handpiece , Battery charger, Battery pack, Anti- glare shield, Light guide, AC/DC adapter | | | Chemical composition of patient contacting portions of the device | Disposable sheath (FDA cleared barrier sheath, K132953/ TIDIShieldTM Curing Light Sheath) | | | Disposable sheath (FDA cleared barrier sheath) | | | Technical Specifications - Light intensity | Max. 1,800mW/cm² (±10%) | Max. 2,700mW/cm² (±10%) | Max. 2,700mW/cm² (±10%) | Max. 2,000mW/cm² (±10%) | Max. 3,000mW/cm² (±10%) | | Technical Specifications - Wavelength range | 430 ~ 490nm | | | 430 ~ 490nm | | | Technical Specifications - Peak wavelength- | 460nm | | | 460nm | | | Compliance to FDA- | IEC 60601-1:2005 + A1:2012 IEC 60601-1-2:2007 | | | IEC 60601-1:2005 IEC 60601-1-2:2007 | | | Recognized Standards | ADA/ANSI Specification No.48, ANSI/ADA Standard No. 48-2 | | | ADA/ANSI Specification No.48, ANSI/ADA Standard No 48-2 | | {6}------------------------------------------------ Image /page/6/Picture/0 description: The image shows the logo for "Dentall". The word "Dental" is in bold, black font, with a light purple swoosh above the "D". To the right of "Dental" is the word "all" in white font, set against a green parallelogram. {7}------------------------------------------------ Image /page/7/Picture/0 description: The image shows the logo for "Dentall". The word "Dental" is written in a bold, black font. The "all" portion of the word is written in a light green color and is slanted to the right. There is a light purple shadow behind the word "Dental". #### 7.1 The same between the subject device and the predicate devices. 1) Product Code and Regulatory Classification : The proposed classification of the subject devices is 2 according to the product code, EBZ. It is the same as the predicate devices (K140432). #### 2) Indications for Use : The proposed indications for use of the subject devices is for light curing polymerization of dental composites, luting materials, cements and other light cured materials. It is the same as the predicate devices (K140432). #### 3) Principle of Operation : The subject devices are light-emitting diode (LED) type cordless dental curing light that produce a narrow spectrum of blue light in the 430~490nm range, which is useful energy range for activating the CPQ molecule, most commonly used to initiate the photo polymerization of dental monomers. It is the same as the predicate devices (K140432). 4) Light Source {8}------------------------------------------------ Image /page/8/Picture/0 description: The image shows the logo for "Dentall". The word "Dentall" is written in a bold, sans-serif font. The "Dent" portion of the word is in black, while the "all" portion is in white against a green parallelogram. There is a light purple swoosh above the word "Dent". : The subject device uses 10W LED that produce a narrow spectrum of blue light in the 430~490nm wave range and 460nm peak wavelength. It is the same as the predicate devices (K140432). 5) Power Source : The subject device is handpiece type using an internal rechargeable lithium ion battery (3.7Vdc. 2200mAh) and a battery charger (AC/DC Adapter, Input: 100-240Vac, 50/60 Hz, 400 mA Output: 5.0Vdc, 1.6A) is provided by manufacturer. It is the same as the predicate devices (K140432). 6) Chemical composition of patient contacting portions of the device : The subject device uses a disposable sheath (FDA cleared barrier sheath, K132953/TIDIShiela™ Curing Light Sheath). It is the same as the predicate devices (K140432). #### 7.2 Differences between Subject Devices and Predicates Devices 1) Operation Modes and Light Intensity : The subject devices have several modes corresponding to the light output intensity and available times. The light output safety and performance test was conducted according to IEC 60601-1, ANSI/ADA specification no.42, ANSI/ADA specification no. 42-2 and FDA guidance performance testing requirements with the difference. The testing results show that these difference do not raise any problems in the safety and performance. #### 2) Depth of cure : The subject devices specify several depth of cure corresponding to the operation mode. The depth of cure was evaluated according to ANSI/ADA specification no.42, ANSI/ADA specification no. 42-2 and FDA guidance performance testing requirements with the difference. The testing results show that these difference do not raise any problems in the safety and performance. ## 8. Electrical Safety and Electromagnetic compatibility The Electrical Safety and Electromagnetic compatibility tests were performed in accordance with the following standards. - IEC 60601-1:2005+A1:2012 and US Deviation (AAMI/ANSI ES 60601-1: 2005+A1: 2012), -Medical electrical equipment - Part 1: General requirements for basic safety and essential performance - -IEC 60601-1-2: 2007, Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances -Requirements and tests The test results conformed to the standards. # 9. Performance Testing - Nonclinical Testing {9}------------------------------------------------ Image /page/9/Picture/0 description: The image shows the logo for Dentalall. The word "Dental" is written in a bold, black font, with a light purple swoosh above it. The word "all" is written in a green box that is tilted to the right. The following non-clinical tests were conducted to evaluate the functionality, performance and substantial equivalence. - -Irradiation (Optical Power Testing) - Spectral irradiance plot (Wavelength Spectrum Testing) - - -Depth of cure (Composite Hardness Testing) The tests are in accordance with the following standards. - American National Standard/American Dental Association (ANSI/ADA) Specification No. 48: -2004, Reaffirmed 2015, Visible Light Curing Units - -American National Standard/American Dental Association (ANSI/ADA) Specification No. 48-2: 2010, Reaffirmed 2015, LED Curing Lights - FDA Guidance for Industry and FDA Staff, Dental Curing Lights -Premarket Notification -510(k) Submissions, Clause 8. Performance Specifications The test results conformed to the requirements of the standards. #### 10. Conclusion In comparing between the subject devices and the predicate devices, there are the same product code, regulatory classification, indications for use, principle of operation, light source, power source, and chemical composition of patient contacting portions. Safety and performance testing supports substantial equivalence of the subject device to the predicate devices.