Who is the manufacturer of Illusion Aligner Pro: Illusion Aligner FLX?

Laxmi Dental Export Pvt., Ltd. filed the 510(k) submission for Illusion Aligner Pro: Illusion Aligner FLX (K233356).

What is the FDA product code for Illusion Aligner Pro: Illusion Aligner FLX?

NXC. It is classified under 21 CFR 872.5470 as a Class 2 device in the Dental panel.

What is the regulatory pathway for Illusion Aligner Pro: Illusion Aligner FLX?

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

What are the predicate devices for Illusion Aligner Pro: Illusion Aligner FLX?

DailyMate Orthodontic Aligner System (K212803); Smylio Invisible Clear Aligners (K212660).

Who can help prepare an FDA 510(k) submission like Illusion Aligner Pro: Illusion Aligner FLX?

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.

Illusion Aligner Pro: Illusion Aligner FLX

K233356 · Laxmi Dental Export Pvt., Ltd. · NXC · Aug 8, 2024 · Dental

Device Facts

Record ID	K233356
Device Name	Illusion Aligner Pro: Illusion Aligner FLX
Applicant	Laxmi Dental Export Pvt., Ltd.
Product Code	NXC · Dental
Decision Date	Aug 8, 2024
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 872.5470
Device Class	Class 2
Attributes	Therapeutic

Intended Use

The Illusion Aligners Pro and Illusion Aligner Flx are indicated for use in the alignment of permanent teeth (i.e., all second molars) through orthodontic treatment of misalignment and malocclusion.

Device Story

Intraoral thermoplastic aligners; prescribed by dentists/orthodontists for orthodontic tooth movement. Input: intraoral scans or physical impressions of patient dentition. Process: 3Shape Ortho System software used for treatment planning; 3D printer creates sequential models representing incremental tooth positions; thermoforming equipment shapes plastic sheets over models. Output: series of sequential aligners worn 20-22 hours/day. Operation: patient wears aligners in sequence; removed for eating/cleaning. Clinical context: clinician monitors treatment from delivery to completion. Benefit: progressive tooth realignment via continuous gentle force.

Clinical Evidence

No clinical data. Biocompatibility testing performed per ISO 10993-5:2009 (In Vitro Cytotoxicity), ISO 10993-10:2021 (Skin Sensitization), and ISO 10993-23:2021 (Intracutaneous Reactivity).

Technological Characteristics

Intraoral thermoplastic appliances. Illusion Aligner Pro: polyurethane. Illusion Aligner Flx: co-polyester and polyurethane composite. Thickness: 0.8 mm. Weight: 10 grams. Fabrication: 3D printing of models followed by thermoforming. Biocompatibility: ISO 10993 compliant.

Indications for Use

Indicated for alignment of permanent teeth (including second molars) in patients requiring orthodontic treatment for misalignment and malocclusion.

Regulatory Classification

Identification

An orthodontic plastic bracket is a plastic device intended to be bonded to a tooth to apply pressure to a tooth from a flexible orthodontic wire to alter its position.

Predicate Devices

DailyMate Orthodontic Aligner System (K212803)
Smylio Invisible Clear Aligners (K212660)

Related Devices

K213026 — Clear Aligner · Shenzhen Meiming Dentistry Technology Co., Ltd. · Aug 16, 2022
K192767 — Clear Aligner · Royal Dental Lab · Jan 8, 2020
K210373 — Clear Aligners · Shenzhen Yinuo Dental Technology Co.Ltd · Aug 27, 2021
K190003 — Vivid Aligners · Orthodent Laboratory, Inc. · Nov 6, 2019
K211537 — QuickAligners · Oral Image, Inc. · Oct 26, 2021

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services logo on the left and the FDA acronym along with the full name of the agency on the right. The FDA part of the logo is in blue, with the acronym in a square and the full name written out to the right of the square. August 8, 2024 Laxmi Dental Export PVT. LTD % Jennifer Day Regulatory Consultant Prime Path Medtech 811 Lakeview Dr. Shoreview, Minnesota 55126 Re: K233356 Trade/Device Name: Illusion Aligner Pro: Illusion Aligner FLX Regulation Number: 21 CFR 872.5470 Regulation Name: Orthodontic Plastic Bracket Regulatory Class: Class II Product Code: NXC Dated: September 29, 2023 Received: September 29, 2023 Dear Jennifer Day: 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 (the 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 available 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. {1}------------------------------------------------ Additional information about changes that may require a new premarket notification are provided in the FDA guidance documents entitled "Deciding When to Submit a 510(k) for a Change to an Existing Device" (https://www.fda.gov/media/99812/download) and "Deciding When to Submit a 510(k) for a Software Change to an Existing Device" (https://www.fda.gov/media/99785/download). Your device is also subject to, among other requirements, the Quality System (QS) regulation (21 CFR Part 820), which includes, but is not limited to, 21 CFR 820.30. Design controls; 21 CFR 820.90. Nonconforming product; and 21 CFR 820.100, Corrective and preventive action. Please note that regardless of whether a change requires premarket review, the QS regulation requires device manufacturers to review and approve changes to device design and production (21 CFR 820.30 and 21 CFR 820.70) and document changes and approvals in the device master record (21 CFR 820.181). 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 Part 803) for devices or postmarketing safety reporting (21 CFR Part 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 Part 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR Parts 1000-1050. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 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). {2}------------------------------------------------ Sincerely, # Michael E. Adjodha -S Michael E. Adjodha, MChE, RAC, CQIA Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT, and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health Enclosure {3}------------------------------------------------ # Indications for Use 510(k) Number (if known) K233356 Device Name Illusion Aligner Pro Illusion Aligner Flx Indications for Use (Describe) Illusion Aligners Pro are indicated for use in the alignment teeth (i.e. all second molars) through orthodontic treatment of misalignment and malocclusion. Illusion Aligner Flx are indicated for use in the alignment teeth (i.e. all second molars) through orthodontic treatment of misalignment and malocclusion. | Type of Use (Select one or both, as applicable) | | |------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------| | 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 Laxmi Dental Export PVT. LTD. The logo consists of the letters "LD" in a stylized font. The "L" is in black, and the "D" is in red. To the right of the letters is the company name, "LAXMI DENTAL EXPORT PVT. LTD.", with "LAXMI" in red and the rest of the text in black. # K233356 # 510(k) Summary This Traditional 510(k) Summary information is being submitted in accordance with Title 21, CFR Section 807.92. #### 1. SUBMITTER | Name of Manufacturer/Owner of 510(k): | Laxmi Dental Exports Pvt Ltd | |----------------------------------------|-----------------------------------------------------| | | Survey No. 201/1, Village Gundale, Boisar Chillar | | | Highway, Boisar, District – Palghar, India – 401501 | | FDA Establishment Registration Number: | 3004793856 | | Primary Contact Person: | Samee Merchant | | Email Address | sameer@laxmidental.com | | Phone Number | 022 - 61437900 | | Fax Number | 022 - 61437999 | | Date of Summary Prepared | 7/9/2024 | #### 2. PURPOSE OF THIS SUBMISSION This submission seeks clearance for the Illusion Aligner Pro and Illusion Aligner Flx; they are substantially equivalent to DailyMate Orthodontic Aligner System (K212803) and Smylio Invisible Clear Aligners (K212660), respectively. #### 3. SUBJECT DEVICES Device Name: Illusion Aligner Pro Common Name or Usual Name: Aligner, Sequential Classification Name: Orthodontic plastic bracket (21 CFR 872.5470) Regulatory Class: II (21 CFR 872.5470) Product Code: NXC (21 CFR 872.5470) Device Name: Illusion Aligner Flx Common Name or Usual Name: Aligner, Sequential Classification Name: Orthodontic plastic bracket (21 CFR 872.5470) Regulatory Class: II (21 CFR 872.5470) Product Code: NXC (21 CFR 872.5470) {5}------------------------------------------------ Image /page/5/Picture/0 description: The image shows the logo for Laxmi Dental Export Pvt. Ltd. The logo consists of a stylized letter "L" in black, followed by a stylized letter "D" in red. To the right of the letters, the text "LAXMI DENTAL EXPORT PVT. LTD." is written in a smaller, sans-serif font. The text is arranged in three lines, with "LAXMI" in red and the rest of the text in black. #### 4. PREDICATE DEVICES Illusion Aligner Pro – Predicate Devices Predicate Device 510(K) Number: K212803 Predicate Device Name: DailyMate Orthodontic Aligner System Common Name or Usual Name: Aligner, Sequential Classification Name: Orthodontic plastic bracket (21 CFR 872.5470) Regulatory Class: II (21 CFR 872.5470) Product Code: NXC (21 CFR 872.5470) Manufacturer: 3D Global Biotech Inc # Illusion Aligner Flx - Predicate Devices Predicate Device 510(K) Number: K212660 Predicate Device Name: Smylio Invisible Clear Aligners Common Name or Usual Name: Aligner, Sequential Classification Name: Orthodontic plastic bracket (21 CFR 872.5470) Regulatory Class: II (21 CFR 872.5470) Product Code: NXC (21 CFR 872.5470) Manufacturer: SMYLIO, INC. #### INDICATIONS FOR USE ട. The Illusion Aligners Pro and Illusion Aligner Flx are indicated for use in the alignment of permanent teeth (i.e., all second molars) through orthodontic treatment of misalignment and malocclusion. #### DEVICE DESCRIPTION 6. A dental health professional (e.g., an orthodontist or a dentist) prescribes the Illusion Aligners Pro and Illusion Aligner Flx are based on an assessment of the patient's teeth. The dental health professional (dentist/orthodontist) takes either the intraoral scans or physical impressions of the patient's teeth, determines the required corrections to align the teeth, and 3Shape's Ortho System is used for treatment planning. Illusion Aligners Pro and Illusion Aligner Flx are intraoral thermoplastic appliances that are worn 20 to 22 hours per day and are designed to be used in a sequence, each aligner providing a gentle continuous force, to allow for the movement of teeth to the final desired position. The aligners are to be removed for eating and for cleaning. Illusion Aligners Pro and Illusion Aligner Flx are fabricated using a three- step process. {6}------------------------------------------------ Image /page/6/Picture/0 description: The image shows a logo for Laxmi Dental Export PVT. LTD. The logo consists of the letters "L" and "D" in a stylized font. The "L" is in black, and the "D" is in red. To the right of the letters is the text "LAXMI DENTAL EXPORT PVT. LTD." in a smaller font. The first step is to obtain the dimensions and details of the patient's dentition. This is generally done using an intraoral scan or a physical impression. This scanned data (digital CAD/CAM models or patient models) is imported into specialized dental software for treatment planning. The second step is the printing of 3D models of the treatment plan for use in step 3 (thermoforming). In the second step, Illusion Aligners Pro and Illusion Aligner Flx utilizes a software application to plan the treatment by creating a series of sequential models that gradually position the teeth into their final desired position. The treatment plan is sent to the doctor for approval. Upon approval, a 3D printer is used to create the models needed for each treatment step to provide the surface around which the aligner is thermoformed. The final step is the thermoforming of a plastic sheet material to each of the sequential treatment steps. This process is done using standard thermoforming equipment and the appropriate material as specified. The trays are provided to the dental health care professional who provides them to the patient in sequential stages, confirming fit and design. The dental health professional monitors treatment from the moment the first aligner is delivered to when the final aligner is finished, and treatment is complete #### TECHNOLOGICAL CHARACTERISTICS 7. A comparison of the relevant technological characteristics between the subject and primary predicate devices is provided in table-1 that follows. #### 8. MATERIALS The Illusion Aligners Pro is made up of polyurethane while Illusion Aligner Flx is made up of copolyester and polyurethane composite. The thickness and weight of the test item is 0.8 mm and 10 grams respectively. The DailyMate aligners are produced from polyurethane. The Smylio Invisible Clear Aligners are produced from co-polyester and polyurethane composite. #### 9. COMPARISON WITH THE PREDICATE DEVICES The Illusion Aligners Pro and the predicate device (DailyMate) consist of the same ingredients. They have the same intended use, similar designs, and performance, and meet the biocompatibility requirements. The Illusion Aligner Flx and the predicate device (Smylio Invisible Clear Aligners) consist of the same ingredients. They have the same intended use, similar designs, and performance, and meet the biocompatibility requirements. The table below compares the subject device to the predicate and reference devices. # Table-1. Illusion Aligners Pro predicate comparison table. {7}------------------------------------------------ Image /page/7/Picture/0 description: The image contains a logo for Laxmi Dental Export PVT. LTD. The logo consists of the letters "LD" in a stylized font, with the "L" in black and the "D" in red. To the right of the letters, the words "LAXMI DENTAL" are written in red, with "EXPORT PVT. LTD." written in black below it. | Comparison Parameters | Subject Device (Illusion Aligners Pro) | Predicate Device (DailyMate aligners) | |--------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | 510K Number | K233356 | K212803 | | Indication for Use | The Illusion Aligners Pro is indicated for use in the alignment of permanent teeth (i.e., all second molars) through orthodontic treatment of misalignment and malocclusion | The DailyMate Orthodontic Aligner System is indicated for the treatment of tooth malocclusion in patients with permanent dentition. The aligner system repositions teeth by way of continuous gentle force. | | Product Code | NXC | NXC | | Intended Population | Individuals with permanent dentition | Individuals with permanent dentition | | OTC or Rx | Rx | Rx | | Raw Material Used | Polyurethane | Polyurethane | | Mode of Action | The aligner is an orthodontic appliance intended for intra-oral use. Individual devices will be used between 20 - 22 hours per day for a period ranging from one to three weeks The corrective forces to align teeth are primarily generated by the difference between the starting tooth position and the planned tooth position defined by the tray. | Based on the clinician's treatment plan, each aligner is used for a defined period of time to exert gentle force to achieve progressive realignment of the teeth. This occurs over time until the final correction has been achieved. | {8}------------------------------------------------ Image /page/8/Picture/0 description: The image shows the logo for Laxmi Dental Export PVT. LTD. The logo consists of the letters "L" and "D" in a stylized font. The "L" is in black, and the "D" is in red. To the right of the letters is the company name, "LAXMI DENTAL EXPORT PVT. LTD.", with "LAXMI" in red and the rest of the text in black. | Comparison Parameters | Subject Device (Illusion Aligner Flx) | Predicate Device (Smylio Invisible Clear Aligners) | |----------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | 510K Number | K233356 | K212660 | | Indication for Use | The Illusion Aligner Flx is indicated for use in the alignment of permanent teeth (i.e., all second molars) through orthodontic treatment of misalignment and malocclusion | The Smylio Invisible Clear Aligners is indicated for the alignment of teeth during orthodontic treatment of malocclusion. | | Product Code | NXC | NXC | | Intended Population | Individuals with permanent dentition | Individuals with permanent dentition | | Mode of Action | Orthodontic tooth movement occurs through forces applied by the device to the dentition as each tooth follows the programmed displacement based on a doctor's prescription | Orthodontic tooth movement occurs through forces applied by the device to the dentition as each tooth follows the programmed displacement based on a doctor's prescription | | OTC or Rx | Rx | Rx | | Raw Material Used | Co-polyester and polyurethane composite | Thermoplastic polyurethane polyester composite resin | | Anatomical Site of Use | Oral Cavity | Oral Cavity | | Mode of Action /Operating Principle | The aligner is an orthodontic appliance intended for intra-oral use. Individual devices will be used between 20 – 22 hours per day for a period ranging from one to three weeks The corrective forces to align teeth are primarily generated by the difference between the starting tooth position and the planned tooth position defined by the tray. | Continuous gentle force applied to teeth following the prescribed and approved treatment plan to achieve orthodontic movement | - # Table-2. Illusion Aligners Flx predicate comparison table. {9}------------------------------------------------ Image /page/9/Picture/0 description: The image shows the logo for Laxmi Dental Export PVT. LTD. The logo consists of a stylized letter "L" in black, followed by a red shape resembling a "D". To the right of these shapes, the text "LAXMI DENTAL EXPORT PVT. LTD." is displayed in a simple, sans-serif font. #### 10. SUBSTANTIAL EQUIVALENCE DISCUSSION Illusion Aligners Pro and Illusion Aligner Flx have been subjected to ISO 10993 biocompatibility studies to demonstrate the device is as safe as its predicate device. The performance tests were conducted to demonstrate that the subject device is as effective as its predicate device. ## Biocompatibility Testing Per ISO 10993-1: 2018, Illusion Aligner Pro and Illusion Aligner Flx direct tissue-contacting, surface device contacting mucosal membrane for > 30 days due to treatment consisting of multiple aligners worn for 7 days consecutively. Thus, the aligners are permanent tissue contacting devices. The subject device was evaluated for: In Vitro Cytotoxicity (ISO 10993-5:2009) Skin Sensitization (ISO 10993-10: 2021) Intracutaneous Reactivity (ISO 10993-23:2021) ## Clinical Studies No clinical study was conducted. #### 11. CONCLUSIONS Based on the comparison analysis, performance tests, biocompatibility tests and animal study provided in this submission, the subject device, Illusion Aligners Pro and Illusion Aligner Flx are demonstrated to be as safe and effective as the legally marketed predicate device, DailyMate aligners and Smylio Invisible Clear Aligners. So, the subject devices are considered Substantially Equivalent (SE) to the predicate devices.