(45 days)
No
The device description and intended use clearly indicate it is a dental restorative material (resin) and a bonding agent, with no mention of AI or ML technology. The "Mentions AI, DNN, or ML" section explicitly states "Not Found".
No
The device is described as a tooth shade resin material intended to restore defects in teeth, which is a restorative rather than a therapeutic function.
No
This device is a tooth shade resin material intended to restore defects in teeth, which is a therapeutic function, not a diagnostic one.
No
The device description explicitly states it is a "device composed of materials such as bisphenol A glycidylmethacrylate (Bis-GMA)" and is intended to restore defects in teeth, indicating it is a physical material, not software.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is for restoring carious or structural defects in teeth. This is a direct treatment applied to the patient's body, not a test performed on a sample taken from the body to diagnose a condition.
- Device Description: The device is described as a "Tooth shade Resin Material" composed of materials like bisphenol A glycidylmethacrylate (Bis-GMA) intended to restore teeth. This aligns with a dental restorative material, not an IVD.
- CFR Classification: The device is classified under CFR 29 Section 872.3690, which is for "Tooth shade Resin Material." IVDs are classified under different sections of the CFR, typically related to diagnostic tests and laboratory procedures.
- Lack of IVD Characteristics: The description does not mention any characteristics typical of an IVD, such as analyzing biological samples (blood, urine, tissue), detecting biomarkers, or providing diagnostic information.
In summary, the CLEARFIL AP-X PLT INTRO KIT is a dental restorative material used for treating teeth directly, not a device used for in vitro diagnostic testing.
N/A
Intended Use / Indications for Use
The intended uses of this device are as follows. They are the same as CLEARFIL AP-X manufactured by Kuraray Medical Inc.
- Class I, II, V restorations of posterior teeth 1)
- Class III, IV, V restorations of anterior teeth 2)
-
- Cervical cavities or defects involving root surfaces
CLEARFIL AP-X PLT INTRO KIT is indicated for the following applications:
-
Class I, II, V restorations of posterior teeth
-
Class III, IV, V restorations of anterior teeth
-
Cervical cavities or defects involving root surfaces
Product codes
EBF
Device Description
This product is classified into Tooth shade Resin Material, CFR 29 Section 872.3690, because it is a device composed of materials such as bisphenol A glycidylmethacrylate (Bis-GMA) intended to restore carious or structural defects in teeth.
This device is combination of CLEARFIL AP-X PLT and CLEARFIL SE BOND (K012442). CLEARFIL AP-X PLT is substantially same to CLEARFIL AP-X(K012740) manufactured by Kuraray Medical Inc. on the technological characteristics, chemical ingredients and safety. (K012740). Therefore the technological characteristics, chemical ingredients and safety of CLEARFIL AP-X PLT INTRO KIT are substantially equivalent as the predicate devices.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
teeth
Indicated Patient Age Range
Not Found
Intended User / Care Setting
Not Found
Description of the training set, sample size, data source, and annotation protocol
Not Found
Description of the test set, sample size, data source, and annotation protocol
Not Found
Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Not Found
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
Not Found
Predicate Device(s)
Reference Device(s)
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 872.3690 Tooth shade resin material.
(a)
Identification. Tooth shade resin material is a device composed of materials such as bisphenol-A glycidyl methacrylate (Bis-GMA) intended to restore carious lesions or structural defects in teeth.(b)
Classification. Class II.
0
KURARAY MEDICAL INC.
Image /page/0/Picture/2 description: The image is a black and white logo for Kuraray. The logo features a stylized letter "K" with a geometric design. Below the symbol is the word "KURARAY" in a bold, sans-serif font.
Dental Material Department 3-1-6 Nihonbashi, Chuo-ku, Tokyo 103-8254, Japan Tel : +81.3.3277.6949 - Fax : 510(k) Stoff Mix SRY
OCT 2 4 2002
| 1. Submitter | |
|---|---|
| 1) Name | KURARAY MEDICAL INC. |
| 2) Address | 1621 Sakazu, Kurashiki, Okayama 710-8622, Japan |
| 3) Contact person | Koji Nishida |
| Dental Material Department, Kuraray Medical Inc. |
- Contact person in the U.S.
Masava Sasaki Kuraray America Inc. 101 East 52nd Street, 26th Floor New York, NY 10022 Telephone : (212)-986-2230 (Ext.115) 1-(800)-879-1676 Facsimile : (212)-867-3543 August 25, 2002
- Date
-
- Name of Device
-
- Proprietary Name
-
- Classification Name
-
- Common/Usual Name
CLEARFIL AP-X PLT INTRO KIT Tooth shade resin material (21CFR 872.3690) Composite resin restorative
-
- Predicate device:
The predicate devices are as follows.
- Predicate device:
| 1. CLEARFIL AP-X by Kuraray Medical Inc. | (K012740) |
|---|---|
| 2. CLEARFIL SE BOND by Kuraray Medical Inc. | (K012442) |
-
- Description for the premarket notification
This product is classified into Tooth shade Resin Material, CFR 29 Section 872.3690, because it is a device composed of materials such as bisphenol A glycidylmethacrylate (Bis-GMA) intended to restore carious or structural defects in teeth.
- Description for the premarket notification
-
- Statement of the intended use
The intended uses of this device are as follows. They are the same as CLEARFIL AP-X manufactured by Kuraray Medical Inc.
- Statement of the intended use
-
Class I, II, V restorations of posterior teeth 1)
-
Class III, IV, V restorations of anterior teeth 2)
-
- Cervical cavities or defects involving root surfaces
6. Statement of the technological characteristics and safety
This device is combination of CLEARFIL AP-X PLT and CLEARFIL SE BOND (K012442). CLEARFIL AP-X PLT is substantially same to CLEARFIL AP-X(K012740) manufactured by Kuraray Medical Inc. on the technological characteristics, chemical ingredients and safety. (K012740). Therefore the technological characteristics, chemical ingredients and safety of CLEARFIL AP-X PLT INTRO KIT are substantially equivalent as the predicate devices.
1
DEPARTMENT OF HEALTH & HUMAN SERVICES
Image /page/1/Picture/1 description: The image shows the seal of the Department of Health & Human Services - USA. The seal features a stylized image of three human profiles facing right, stacked on top of each other. The profiles are black and have a flowing, abstract design. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the image.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
OCT 2 4 2002
Kuraray Medical. Incorporated C/O Ms. Masaya Sasaki Kuraray America, Incorporated 101 East 52nd Street, 26th Floor New York, New York 10022
Re: K022999
Trade/Device Name: CLEARFIL AP-X PLT Intro Kit Regulation Number: 21 CFR 872.3690 Regulation Name: Tooth-Shade Resin Material Regulatory Class: II Product Code: EBF Dated: September 04, 2002 Received: September 09, 2002
Dear Ms. Sasaki:
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.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such 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.
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.
2
Page 2 - Ms. Masaya Sasaki
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); 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.
This letter will allow you to begin marketing your device as described in your Section 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus. permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 21 CFR Part 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4613. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html
Sincerely vours
Timbthy Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
3
Device Name: CLEARFIL AP-X PLT INTRO KIT
510(k) Number (if known):
Indications for Use
CLEARFIL AP-X PLT INTRO KIT is indicated for the following applications:
-
Class I, II, V restorations of posterior teeth
-
Class III, IV, V restorations of anterior teeth
-
Cervical cavities or defects involving root surfaces
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use______________________________________________________________________________________________________________________________________________________________
Over-The-Counter Use__________________________________________________________________________________________________________________________________________________________
(Optional Format 1-2-96)
Asher DVS for Dr Susan Kemner
OR
ision of Anesthesiology, General Hospital, Infection Control, Dental Devices 510(k) Number