(91 days)
Not Found
No
The summary describes standard image processing software for dental radiographs and does not mention AI, ML, or related concepts.
No
The device is described as an X-ray system intended for examination and diagnosis, which are diagnostic purposes, not therapeutic ones.
Yes
The "Intended Use / Indications for Use" section explicitly states that the device is "intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw and supporting oral structures."
No
The device description explicitly states it is a "host PC powered device" and processes images captured from a "sensor device that is placed in a patient's mouth." This indicates the system includes hardware components (PC, sensor) in addition to the software.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- IVD Definition: In vitro diagnostics are tests performed on samples taken from the human body, such as blood, urine, or tissue, to detect diseases, conditions, or infections. They are used to provide information for diagnosis, monitoring, or screening.
- Device Function: The description clearly states that this device is an "extra-oral source x-ray system" that produces "digital radiographs" for "dental radiographic examination and diagnosis of diseases of the teeth, jaw and supporting oral structures." This involves using radiation to create images of internal structures, not analyzing samples taken from the body.
- Input: The input is "digital radiographs," which are images, not biological samples.
- Anatomical Site: The anatomical site is "teeth, jaw and supporting oral structures," which are internal structures being imaged, not the source of a biological sample.
The device is a medical imaging system used for diagnosis based on visual interpretation of X-ray images, not an in vitro test.
N/A
Intended Use / Indications for Use
An extra-oral source x-ray system which is a host PC powered device that produces digital radiographs and is intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw and supporting oral structures.
Product codes (comma separated list FDA assigned to the subject device)
90 MUH
Device Description
The Cleartooth Digital X-Ray System software processes standard dental images captured from a sensor device that is placed in a patient's mouth as if it were dental X-ray film. It provides users with a familiar personal computer moveable window interface, including pushbuttons, tool bars, pull-down menus, and pop-up menus. It allows users to access its features by point and click, and it allows them to work with images using intuitive and responsive features like orienting an image.
Mentions image processing
Yes
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
X-Ray
Anatomical Site
teeth, jaw and supporting oral structures
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): If the device was cleared using the 510(k) pathway, identify the Predicate Device(s) K/DEN number used to claim substantial equivalence and list them here in a comma separated list exactly as they appear in the text. List the primary predicate first in the list.
Reference Device(s): Identify the Reference Device(s) K/DEN number and list them here in a comma separated list exactly as they appear in the text.
Not Found
Predetermined Change Control Plan (PCCP) - All Relevant Information for the subject device only (e.g. presence / absence, what scope was granted / cleared under the PCCP, any restrictions, etc).
Not Found
§ 872.1800 Extraoral source x-ray system.
(a)
Identification. An extraoral source x-ray system is an AC-powered device that produces x-rays and is intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw, and oral structures. The x-ray source (a tube) is located outside the mouth. This generic type of device may include patient and equipment supports and component parts.(b)
Classification. Class II.
0
TAB 4 - SUMMARY
Image /page/0/Picture/3 description: The image shows the logo for "cleartooth electronics". The logo consists of a stylized "C" shape enclosed in a rounded square on the left, followed by the word "cleartooth" in a bold, sans-serif font with a trademark symbol. Below "cleartooth" is the word "electronics" in a smaller, sans-serif font.
240 SAINT PAUL STREET SUITE 305 DENVER CO 80206 Phone: 303-733-1999 Fax: 303-733-6268
SUMMARY
Submitter's name:
Cleartooth Electronics, Inc.
Address:
240 St. Paul St., Suite 305 Denver, CO 80206
Phone:
Name of contact person:
303-733-1999
Greg Holland Requlatory Specialists, Inc 3722 Ave. Sausalito Irvine, CA 92606 Phone: 949-262-0411 fax: 949-552-2821
Date the summary was prepared: September 15, 2003
September 15, 2003
Name of the device: | Cleartooth Digital X-Ray System |
---|---|
Trade or proprietary name: | Cleartooth Digital X-Ray System |
Common or usual name: | Extra-oral source x-ray system |
Classification name: | System, x-ray, extra-oral source, digital |
The legally marketed device to which we are claiming equivalence [807.92(a)(3)]:
DXS DIGITAL X-RAY SYSTEM
Description of the device:
The Cleartooth Digital X-Ray System software processes standard dental images captured from a sensor device that is placed in a patient's mouth as if it were dental X-ray film. It provides users with a familiar personal computer moveable window interface, including pushbuttons, tool bars, pull-down menus, and pop-up menus. It allows users to access its features by point and click, and it allows them to work with images using intuitive and responsive features like orienting an image.
1
K33141
Page 2 of 2
Indications:
An extra-oral source x-ray system which is a host PC powered device that produces digital radiographs and is intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw and supporting oral structures.
Summary of the technological characteristics of our device compared to the predicate device:
The predicate DXS Digital X-Ray System K013271 and Cleartooth Digital X-Ray System were compared in the following areas and found to have similar technological characteristics and to be equivalent.
Intended use Indications for use Target population Design Materials Performance Biocompatibility Mechanical safety Chemical safety Anatomical sites Where used Standards met Thermal safety Radiation safety Standards met
2
Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health and Human Services. The logo features a stylized eagle with three stripes 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 9200 Corporate Boulevard Rockville MD 20850
Cleartooth Electronics, Inc. % Mr. Greg Holland Regulatory Specialist Regulatory Specialists, Inc. 3722 Ave. Sausalito IRVINE CA 92606
Re: K033147
Trade/Device Name: Cleartooth Digital X-Ray System Regulation Number: 21 CFR 872.1800 Regulation Name: Extraoral source x-ray system Regulatory Class: II Product Code: 90 MUH Dated: September 29, 2003 Received: October 2, 2003
Dear Mr. Holland:
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. 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.
DEC 3 0 2003
3
Page 2
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), please contact the Office of Compliance at one of the following numbers, based on the regulation number at the top of the letter:
8xx. 1xxx | (301) 594-4591 |
---|---|
876.2xxx, 3xxx, 4xxx, 5xxx | (301) 594-4616 |
884.2xxx, 3xxx, 4xxx, 5xxx, 6xxx | (301) 594-4616 |
892.2xxx, 3xxx, 4xxx, 5xxx | (301) 594-4654 |
Other | (301) 594-4692 |
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) you may obtain. 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 yours,
Nancy C. Brogden
Nancy C. Brogdon Director, Division of Reproductive, Abdominal and Radiological Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
4
Page__________________________________________________________________________________________________________________________________________________________________________
510(k) Number (if known): KD33147
Device Name: Cleartooth Digital X-Ray System
Indications For Use:
An extra-oral source x-ray system which is a host PC powered device that produces digital radiographs and is intended for dental radiographic examination and diagnosis of diseases of the teeth, jaw and supporting oral structures.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEILDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use | ✓ | OR | Over-The-Counter Use |
---|---|---|---|
(Per 21 CFR 801.109) | (Optional Format 1-2-96) |
Nancyc brondon (Division Sign-Off) Division of Reproductive, Abdominal, and Radiological Devices | ||
---|---|---|
REGULATORY SPECIALISTS, INC. | 510(k) Number: K033147 | Page 11 |