(79 days)
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The document describes a dental ceramic material and its application techniques, with no mention of AI or ML.
No
This device is a dental ceramic used by dental technicians to manufacture all-ceramic dental appliances, such as crowns or bridges, for patients. It is a material used in the creation of a restoration, not a therapeutic device itself.
No
The device is a dental ceramic system used by dental technicians to manufacture all-ceramic dental appliances for patients. It is a material for manufacturing restorations, not a tool for diagnosing medical conditions.
No
The device description clearly states it is a dental ceramic system consisting of ceramic powders, which are physical materials, 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 veneering dental frameworks to create dental appliances for individual patients. This is a restorative dental material, not a diagnostic test performed on biological samples.
- Device Description: The description details a dental porcelain system used by dental technicians to manufacture dental restorations. It focuses on the material properties and layering techniques for creating aesthetically pleasing and functional dental prosthetics.
- Lack of Diagnostic Purpose: There is no mention of analyzing biological samples (blood, urine, tissue, etc.) or providing information for the diagnosis, monitoring, or treatment of a disease or condition.
- User: The intended user is a professional dental technician, not a healthcare professional performing diagnostic tests.
The device is clearly intended for the fabrication of dental prosthetics, which falls under the category of medical devices, but not specifically In Vitro Diagnostic devices.
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Intended Use / Indications for Use
Zenoflex dimension is a dental ceramic, which is suitable for veneering hard-sintered zirconium dioxide frameworks with a coefficient of thermal expansion (CTE 25-500°C) of approx. 10.5 x 10 ° K-1.
Product codes (comma separated list FDA assigned to the subject device)
EIH
Device Description
Zenoflex dimension is a dental porcelain system that consists of about 150 different ceramic powders and it is intended to be used by professional dental technicians to manufacture all-ceramic dental appliances for the sole use of particular patients. Zenoflex dimension is recommended for veneering zirconium dioxide (ZrQs) frameworks with a coefficient of thermal expansion [CTE ¿25-500°C]] of approximately 10,5 x 10° Ki¹.
The Zenoflex dimension ceramic offers the dental technician the possibility to chose between different kinds of laver techniques considering aesthetical and economical aspects.
The "One layer technique", which is a fast and simple procedure to manufacture ceramic restorations, considers primarily the economical aspects. For manufacturing ceramic restorations the user needed numerous types of ceramic (dentine and incisal ceramics) so far. But now less types of ceramic are necessary for manufacturing anatomical crowns or bridges and for achieving the desired dental colour.
The "Three layer techniques" enable the user to achieve a dental restoration with a more aesthetical result, because this layer technique comprises the application of at least three different types of ceramic.
With the "Professional layer technique" the dental technician can carry out an extended professional build-up to achieve a dental restoration with the most aesthetical result.
Furthermore the Zenoflex dimension ceramic enables the user to manufacture dental restorations with colours of the "VITA Toothguide Classical" as well as of the "VITA Toothguide 3D-Master".
Mentions image processing
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Mentions AI, DNN, or ML
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Input Imaging Modality
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Anatomical Site
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Indicated Patient Age Range
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Intended User / Care Setting
Professional dental technicians / Not Found
Description of the training set, sample size, data source, and annotation protocol
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Description of the test set, sample size, data source, and annotation protocol
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Summary of Performance Studies (study type, sample size, AUC, MRMC, standalone performance, key results)
Physical, biological and chemical properties of the device, like bending strength, coefficient of thermal expansion, biocompatibility and chemical solubility were tested according to international accepted standards, e.g. ISO 6872, ISO 7405, and meet their demands, respectively, and indicate high safety and effectiveness.
Key Metrics (Sensitivity, Specificity, PPV, NPV, etc.)
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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.
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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).
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§ 872.6660 Porcelain powder for clinical use.
(a)
Identification. Porcelain powder for clinical use is a device consisting of a mixture of kaolin, felspar, quartz, or other substances intended for use in the production of artificial teeth in fixed or removable dentures, of jacket crowns, facings, and veneers. The device is used in prosthetic dentistry by heating the powder mixture to a high temperature in an oven to produce a hard prosthesis with a glass-like finish.(b)
Classification. Class II.
0
MAR 1 6 2011
5. 510 (k) Summary
This 510(k) summary provides the basic principle for determination of substantial equivalence according to 21 CFR Part 807.92.
1. Submitter of 510(k)
| Address: | Wieland Dental + Technik GmbH & Co. KG
Schwenninger Str. 13
D-75179 Pforzheim
Germany |
|-----------------|------------------------------------------------------------------------------------------------|
| Phone: | +49-7231-3705-0 |
| Contact person: | Dr. Gerhard Polzer |
| Phone: | +49-7231-3705-219 |
| Fax: | +49-7231-357959 |
| e-mail: | gerhard.polzer@wieland-dental.de |
2. Device name
Zenoflex dimension Trade name: Common name: Veneering ceramic Classification name: Porcelain powder for clinical use (21 CFR 872.6660, Product code: EIH, Class II)
3. Legally marketed equivalent device
| Predicate device: | Zirox |
|---|---|
| 510(k) number: | K051249 |
12/07/2010 Date of Summary:
1
510 (k) Summarv
4. Description of the Device
Zenoflex dimension is a dental porcelain system that consists of about 150 different ceramic powders and it is intended to be used by professional dental technicians to manufacture all-ceramic dental appliances for the sole use of particular patients. Zenoflex dimension is recommended for veneering zirconium dioxide (ZrQs) frameworks with a coefficient of thermal expansion [CTE ¿25-500°C]] of approximately 10,5 x 10° Ki¹.
The Zenoflex dimension ceramic offers the dental technician the possibility to chose between different kinds of laver techniques considering aesthetical and economical aspects.
The "One layer technique", which is a fast and simple procedure to manufacture ceramic restorations, considers primarily the economical aspects. For manufacturing ceramic restorations the user needed numerous types of ceramic (dentine and incisal ceramics) so far. But now less types of ceramic are necessary for manufacturing anatomical crowns or bridges and for achieving the desired dental colour.
The "Three layer techniques" enable the user to achieve a dental restoration with a more aesthetical result, because this layer technique comprises the application of at least three different types of ceramic.
With the "Professional layer technique" the dental technician can carry out an extended professional build-up to achieve a dental restoration with the most aesthetical result.
Furthermore the Zenoflex dimension ceramic enables the user to manufacture dental restorations with colours of the "VITA Toothguide Classical" as well as of the "VITA Toothguide 3D-Master".
5. Intended Use of the Device
Zenoflex dimension is a dental ceramic, which is suitable for veneering hard-sintered zirconium dioxide frameworks with a coefficient of thermal expansion (CTE 25-500°C) of approx. 10.5 x 10 ° K-1.
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510 (k) Summary
6. Comparison with the predicate device
Zenoflex dimension is substantially equivalent to the medical device Zirox.
Zenoflex dimension as well as Zirox is dental porcelain, which is made of glass frit. Both have similar indications for use, in which they are intended to be used by professional.dental technicians to veneer zirconium dioxide (ZrO2) frameworks to manufacture dental restorations. Physical, biological and chemical properties of the device, like bending strength, coefficient of thermal expansion, biocompatibility and chemical solubility were tested according to international accepted standards, e.g. ISO 6872, ISO 7405, and meet their demands, respectively, and indicate high safety and effectiveness.
Considering these excellent material properties and the numerous similarities as well as the lack of any significant differences between both devices, it can be concluded, that Zenoflex dimension is as safe, as effective, and performs as well as or better than the predicate device.
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Food and Drug Administration 10903 New Hampshire Avenue Document Control Room -WO66-G609 Silver Spring, MD 20993-0002
Gerhard Polzer, Ph.D. Director, Regulatory Affairs Wieland Dental + Technik GmbH & Company KG Schwenninger Strasse 13 D-75179 Pforzheim GERMANY
MAR 1 6 201
Re: K103773
Trade/Device Name: Zenoflex dimension Regulation Number: 21 CFR 872.6660 Regulation Name: Porcelain Powder for Clinical Use Regulatory Class: II Product Code: EIH Dated: December 7, 2010 Received: December 27, 2010
Dr. Polzer:
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- Dr. Polzer
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 (OS) 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/Safetv/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/ResourcesforYou/Industry/default.htm.
Sincerely vours.
Nh for
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): K103773
Device Name: Zenoflex dimension Indications for Use:
Zenoflex dimension is a dental ceramic, which is suitable for veneering hard-sintered zirconium dioxide frameworks with a coefficient of thermal expansion (CTE 25-500°C) of approx. 10.5 x 10° K 1.
Prescription Use × (21 CFR Part 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR Part 807 Subpart C)
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Page 1 of ____________________________________________________________________________________________________________________________________________________________________
Susan Runne
(Division Sign-Off) (Division of Anesthesiology, General Hospital Infection Control, Dental Devices
510(k) Number: K103773