Embrace Pit and Fissure Sealant, Low Fill is a professional dental material, designed with no Bisphenol A, that contains fluoride releasing, light cured, glass-filled acrylate resins and is less than 10% filled. Embrace Pit and Fissure Sealant, Low Fill is available in two shades (tooth-colored and off-white) and is used to seal the pits and fissures in teeth.

Device Description

Embrace Pit and Fissure Sealant, Low Fill is a fluoride releasing, light-cured acrylate resin, with no Bisphenol A, that is less than 10% filled and is available in two shades, tooth-colored and off-white.

AI/ML Overview

Here's an analysis of the provided text regarding the acceptance criteria and supporting study for the "Embrace™ WetBond™ Pit and Fissure Sealant, Low Fill" device:

1. Table of Acceptance Criteria and Reported Device Performance:

The provided document describes performance testing (bench testing) for the device. It does not explicitly state "acceptance criteria" in a pass/fail sense, but rather lists measured performance characteristics which are presumably considered acceptable given the conclusion of substantial equivalence.

Performance Metric	Reported Device Performance
Density / Specific gravity	1.160 g / mL
Working time in ambient light	> 5 minutes
Light cure setting time	20 seconds
Depth of cure after 20 second light cure	1.88 mm
Film thickness	9 µm
Compressive Strength	33,120 ± 3000 p.s.i. / 228 ± 21 MPa
Diametral Tensile Strength	5,365 ± 300 p.s.i. / 37 ± 2 MPa
Film Thickness (repeated entry)	9 µm

2. Sample Size Used for the Test Set and Data Provenance:

The document describes bench testing. It does not specify the sample sizes used for each of the performance metrics. The data provenance is from bench laboratory testing conducted by PULPDENT CORPORATION. It is not clinical data, so terms like "retrospective" or "prospective" for human subjects do not apply here.

3. Number of Experts Used to Establish the Ground Truth for the Test Set and Qualifications of Those Experts:

This information is not applicable as the study described is bench testing of physical/chemical properties, not a study involving human subjects or expert assessment for ground truth.

4. Adjudication Method for the Test Set:

This information is not applicable as the study described is bench testing of physical/chemical properties.

5. If a Multi-Reader Multi-Case (MRMC) Comparative Effectiveness Study was Done:

No, a Multi-Reader Multi-Case (MRMC) comparative effectiveness study was not conducted or described in the provided document. The study focuses on bench testing of material properties.

6. If a Standalone (i.e., algorithm only without human-in-the-loop performance) Study was Done:

No, a standalone study in the context of an algorithm's performance was not conducted or described. This device is a dental material, not an AI or software device.

7. The Type of Ground Truth Used:

The "ground truth" for the bench tests would have been established by standard scientific measurement techniques and established protocols for each material property (e.g., using a universal testing machine for compressive strength, a light meter for cure time, etc.). It's based on objective physical and chemical measurements, not expert consensus, pathology, or outcomes data in a clinical sense.

8. The Sample Size for the Training Set:

This information is not applicable. There is no "training set" as this is a physical product undergoing bench testing, not a machine learning model.

9. How the Ground Truth for the Training Set was Established:

This information is not applicable as there is no training set.

Summary

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113818 PULPDENT CORPORATION

MAR 2 1 2012

80 Oakland Street Watertown. MA 02472 USA

TEL: 617-926-6666 FAX: 617-926-6262 Pulpdent@pulpdent.com

510(k) Summary

Kenneth J. Berk 80 Oakland Street PO Box 780 Watertown. MA 02472 USA

617-926-6666 Telephone: Fax: 617-926-6262 ken@pulpdent.com

DEVICE:

Trade Name: Embrace™ WetBond™ Pit and Fissure Sealant, Low Fill Classification Name: Pit and Fissure Sealant and Conditioner FDA Product Code: 76 EBC, 21 CFR Part 872.3765

PREDICATE DEVICES:

Pulpdent Embrace™ WetBond™ Pit and Fissure Sealant Pulpdent Embrace™ Clear Sealant

DESCRIPTION:

INTENDED USE:

Embrace Pit and Fissure Sealant, Low Fill is used by dental professionals to seal the pits and fissures in teeth.

COMPARISON WITH PREDICATE PRODUCTS:

Embrace Pit and Fissure Sealant, Low Fill is substantially equivalent in design, composition, performance and intended use to the predicate products. The predicate products have been found substantially equivalent under the 510(k) Premarket Notification process as Class II Dental Devices under CFR 872.3765.

A summary of the comparison:

PRODUCT	DESCRIPTION	INTENDED USE	COMPOSITION
Embrace Pit and FissureSealant, Low Fill	Fluoride releasing, light cured,acrylate resins	Seal the pits and fissures in teeth	Acrylate resinsPhoto-chemistry
Embrace Pit and FissureSealantK020287	Fluoride releasing, light cured,glass-filled acrylate resins	Seal the pits and fissures in teeth	Acrylate resinsPhoto-chemistryGlass filler
Embrace Clear SealantK052281	Fluoride releasing, light cured,acrylate resins	Seal the pits and fissures in teeth	Acrylate resinsPhoto-chemistry

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PULPDENT CORPORATION

80 Oakland Street Watertown, MA 02472 USA .

TEL: 617-926-6666 FAX: 617-926-6262 Pulpdent@pulpdent.com

510(k) Summary

SUMMARY OF PERFORMANCE TESTING - Bench

The following test results demonstrate that Embrace Pit and Fissure Sealant, Low Fill performs as intended:

Density / Specific gravity	1.160 g / mL
Working time in ambient light	> 5 minutes
Light cure setting time	20 seconds
Depth of cure after 20 second light cure	1.88 mm
Film thickness	9 µm
Compressive Strength	33,120 ± 3000 p.s.i. / 228 ± 21 MPa
Diametral Tensile Strength	5,365 ± 300 p.s.i. / 37 ± 2 MPa
Film Thickness	9 µm

CONCLUSION:

From the above comparisons, the bench testing, a search of the relevant scientific literature and the organizational experience with Embrace resins, it can be concluded that Embrace Pit and Fissure Sealant, Low Fill is substantially equivalent in design, composition, performance and intended use to the predicate products. The predicate products have been found substantially equivalent under the 510(k) Premarket Notification process as Class II Dental Devices under CFR 872.3765 and have been used by dental professionals for more than ten years with no reports of adverse events.

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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three swooping lines forming its body and wings. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the eagle.

Public Health Service

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

MAR 2 1 2012

Mr. Kenneth J. Berk Director of Research Pulpdent Corporation 80 Oakland Street Watertown, MA 02472

Re: K113818

Trade/Device Name: Embrace" Wetbond™ Pit and Fissure Sealant, Low Fill Regulation Number: 21 CFR 872.3765 Regulation Name: Pit and Fissure Sealant and Conditioner Regulatory Class: II Product Codes: EBC Dated: December 21, 2011 Received: December 30, 2011

Dear Mr. Berk:

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. Berk:

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 go to http://www.fda.gov/AboutFDA/CentersOffices/CDRH/CDRHOffices /ucm115809.htm for the Center for Devices and Radiological Health's (CDRH's) Office of Compliance. 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,

Nh foc

Anthony D. Watson, B.S., M.S., M.B.A. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health

Enclosure

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Indications for Use

510(k) Number (if known):

Device Name: Pulpdent Embrace™ WetBond™ Pit and Fissure Sealant, Low Fill

Indications For Use:

Prescription Use X (Part 21 CFR 801 Subpart D) AND/OR

Over-The-Counter Use (21 CFR 807 Subpart C)

(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)

Concurrence of CDRH, Office of Device Evaluation (ODE)

Susan Runai

(Division Sign-Off) Division of Anesthesiology, General Hospital Infection Control, Dental Devices

Page 1 of 1

510(k) Number.

1,10

Regulation Number and Section

§ 872.3765 Pit and fissure sealant and conditioner.

(a)
Identification. A pit and fissure sealant and conditioner is a device composed of resin, such as polymethylmethacrylate, intended for use primarily in young children to seal pit and fissure depressions (faults in the enamel) in the biting surfaces of teeth to prevent cavities.(b)
Classification. Class II.