← Product Code [ELW](/productcode/ELW) · K132599

# SMILEBOND SYSTEM (K132599)

_Millennium Company, LLC · ELW · Feb 25, 2014 · Dental · SESE_

**Canonical URL:** https://fda-staging.innolitics.com/device/K132599

## Device Facts

- **Applicant:** Millennium Company, LLC
- **Product Code:** [ELW](/productcode/ELW.md)
- **Decision Date:** Feb 25, 2014
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 872.3660
- **Device Class:** Class 2
- **Review Panel:** Dental

## Indications for Use

Fast-Set Bite Registration Material is intended for the enhancement of the smile and bite alignment. SmileBond System is intended for . cosmetic correction; . malpositioned teeth: tooth discoloration, incorrect shading; . . anatomical malformation; attrition, abrasion, erosion; and . . decay repair.

## Device Story

SmileBond System is a dental impression material used for cosmetic and functional dental procedures. The device consists of a silicone-based impression material delivered via a dual-barrel cartridge system. It is applied by dental professionals into an impression tray or directly onto the patient's teeth to capture anatomical structures. The material reproduces fine detail for study models or the fabrication of restorative prosthetic devices. In the lab, the clear material is used to create an accurate impression of a final wax-up, which is then transferred to the patient's mouth for the bonding process. The system aids in addressing conditions such as malpositioned teeth, discoloration, anatomical malformations, and decay repair, ultimately facilitating smile enhancement and bite alignment.

## Clinical Evidence

No clinical data. The device relies on substantial equivalence to legally marketed predicate devices based on technological characteristics and intended use.

## Technological Characteristics

Silicone-based impression material; medium viscosity; dual-barrel cartridge delivery system. Class II device under 21 CFR 872.3660. No specific material standards or software algorithms described.

## Regulatory Identification

Impression material is a device composed of materials such as alginate or polysulfide intended to be placed on a preformed impression tray and used to reproduce the structure of a patient's teeth and gums. The device is intended to provide models for study and for production of restorative prosthetic devices, such as gold inlays and dentures.

## Special Controls

*Classification.* Class II (Special Controls).

## Predicate Devices

- Silicone Impression Material ([K801830](/device/K801830.md))
- TempSpan Clear Matrix Material ([K120013](/device/K120013.md))

## Submission Summary (Full Text)

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i32599

# 510(k) Summary

# FEB 2 5 2014

[as required by section 807.92(c)]

This summary of 510(k) safety and effectiveness information is being submitted in accordance with the requirements of SMDA 1990 and 21 CFR § 807.92.

# General Information

| Submitted by:   | Millennium Company LLC<br>2524 Lake Lansing Road<br>Lansing, MI 48912                                                                |
|-----------------|--------------------------------------------------------------------------------------------------------------------------------------|
|                 | Phone: +1 (517) 282-3811<br>Fax: +1 (517) 485-3763<br>Email: drbillv@smilebond.com                                                   |
| Contact Person: | Stephen J. Goldner, JD, RAC<br>Regulatory Affairs Associates, Inc.<br>40701 Woodward Avenue, Suite 102<br>Bloomfield Hills, MI 48304 |
|                 | Phone: +1 (248) 712-0356<br>Fax: +1 (203) 413-4320<br>Email: sgoldner@regaffairs.net                                                 |
| Date Prepared:  | February 6, 2014                                                                                                                     |
| Device Name     |                                                                                                                                      |
| Trade Name:     | Fast-Set Bite Registration Material;<br>SmileBond System                                                                             |
| Common Name(s): | Impression Material                                                                                                                  |
| Classification  |                                                                                                                                      |
| Regulation:     | 21 CFR §872.3660                                                                                                                     |
| Class:          | II                                                                                                                                   |
| Product Code:   | ELW                                                                                                                                  |

Classification Name: Impression material limpression material Regulation Name:

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### Predicate Devices

| Silicone Impression Material          | K801830 | Crown Delta      |
|---------------------------------------|---------|------------------|
| <i>TempSpan</i> Clear Matrix Material | K120013 | Pentron Clinical |

### Device Description

SmileBond System is a patented process for the delivery of dental bonding composites. The SmileBond process is indicated for both cosmetic enhancement of the smile, and functional improvement of the bite (or chewing system).

### Indication for Use

SmileBond Systems Fast Bite Registration Material impression material is indicated for making impressions of the teeth and gums of patients requiring enhancement of the smile and for bite alignment.

### Intended Use

Fast-Set Bite Registration Material is intended for the enhancement of the smile and bite alignment. SmileBond System is intended for

- . cosmetic correction;
- . malpositioned teeth:
- tooth discoloration, incorrect shading; .
- . anatomical malformation;
- attrition, abrasion, erosion; and .
- . decay repair.

### Comparison to Predicate Devices

TempSpan Clear Matrix Material is a clear, medium viscosity vinyl polysiloxane material that reproduces fine detail for the fabrication of extremely accurate provisional restorations

Crown Delta's silicone impression material will be used for making impressions of the teeth and gums of patients requiring models for study and/or for production of restorative prosthetic devices. The impression material is intended to be applied via a dual barrel cartridge system either into an impression tray or directly onto the patient's teeth.

Fast-Set Bite Registration is a silicone impression material intended to be placed on an impression tray to reproduce the structures of the teeth and gums of patients requiring the enhancement of the smile and for bite alignment. The impression material is intended to be applied via a dual barrel cartridge system into an impression tray. The clear impression material is used in the lab to make an accurate impression of the final wax up. Once the impression material is set and slightly modified it is taken to the

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mouth for use in the transfer bonding process.

The Fast Bite Registration Material is manufactured by Crown Delta under its 510(k) K801380 for Millennium Company. The product is labeled with the Own Brand Label (OBL) for SmileBond System.

# Conclusion

The SmileBond System kit is comprised of legally marketed devices. The SmileBond process does not affect the substantial equivalence of the Fast-Set Bite Registration Material to the cited predicate devices.

.

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DEPARTMENT OF HEALTH & HUMAN SERVICES

Image /page/3/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo consists of two main elements: the department's name encircling the image and a stylized symbol. The text reads "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" in a circular arrangement. The symbol is a stylized representation of a human figure, with three curved lines forming the body and head.

Public Health Service

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

February 25, 2014

Millennium Company LLC C/O Mr. Stephen J. Goldner, JD, RAC Regulatory Affairs Associates, Inc. 40701 Woodward Avenue, Suite 102 Bloomfield Hills, MI 48304

Re: K132599

Trade/Device Name: SmileBond System: Fast-Set Bite Registration Material Regulation Number: 21 CFR 872.3660 Regulation Name: Impression Material Regulatory Class: II Product Code: ELW, OFW Dated: November 27, 2013 Received: December 6, 2013

Dear Mr. Goldner:

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.

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Page 2 - Mr. Goldner

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 Small Manufacturers, International and Consumer Assistance at its tollfree number (800) 638-2041 or (301) 796-7100 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" (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 Small Manufacturers, International and Consumer Assistance 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.

Sincerely yours,

Image /page/4/Picture/5 description: The image contains the text "Kwame O. Ulmer-s". The text is arranged in two lines, with "Kwame O." on the top line and "Ulmer-s" on the bottom line. The text is bold and black, and the background is white. The text is slightly distorted.

for

Erin I. Keith, M.S. Acting Division Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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#### DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration

## Indications for Use

Fonn Approved: OMB No. 0910-0120 Expiration Date: December 31, 2013 See PRA Statement on last page.

510(k) Number (if known) K132599

#### Device Name

SmileBond System Fast Bite Registration Material

#### Indications for Use (Describe)

SmileBond Systems Fast Bite Registration material is used for making impressions of the tech and gums of patients requiring enhancement of the smile and for bite alignment.

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

Prescription Use (Part 21 CFR 801 Subpart D)

O Over-The-Counter Use (21 CFR 801 Subpart C)

# PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON A SEPARATE PAGE IF NEEDED.

FOR FDA USE ONLY

| Concurrence of Center for Devices and Radiological Health (CDRH) (Signature) | <div> <p>Mary S. Runner -</p> <p>2014.02.27</p> <p>08:25:13-05'00'</p> </div> |
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| FORM FDA 3881(9/13) | Page 1 of 2 | PSC Publishing Services (301) 443-6740 EF<br>01-001 |
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