(57 days)
Not Found
No
The description focuses on the material properties and manufacturing process of a 3D printing resin for temporary dental restorations. There is no mention of AI or ML in the device description, intended use, or performance studies. The CAD software mentioned is a standard tool for design, not necessarily incorporating AI/ML for the resin itself.
Yes
The device is a light-cured methacrylate-based resin used for the production of temporary dental restorations, which are used to treat and improve the function or appearance of oral structures.
No
The device is a light-cured resin used for 3D printing temporary dental restorations. Its intended use is for treatment (creating a physical dental product), not for diagnosing a condition or disease.
No
The device is a light-cured methacrylate-based resin, which is a physical material used in 3D printing, not a software program.
Based on the provided information, this device is not an In Vitro Diagnostic (IVD).
Here's why:
- Intended Use: The intended use is for creating temporary dental restorations (crowns and bridges) for use in the oral environment. This is a direct application within the body, not for testing samples in vitro (outside the body).
- Device Description: The device is a resin used in a 3D printer to fabricate physical dental restorations. It's a material used to create a medical device, not a test or assay for analyzing biological samples.
- Performance Studies: The performance studies focus on the physical properties of the material, biocompatibility, and manufacturing process validation. These are typical evaluations for a medical device intended for direct patient contact, not for an IVD which would focus on analytical and clinical performance related to a diagnostic test.
IVDs are typically used to examine specimens derived from the human body (like blood, urine, tissue) to provide information for diagnosis, monitoring, or screening. This device does not perform any such function.
N/A
Intended Use / Indications for Use
UltraPrint-Dental Temp C&B UV is indication of temporary dental restorations in conjunction with extra-oral curing light equipment. Duration is not more than 28 days in oral environment.
Product codes (comma separated list FDA assigned to the subject device)
EBG
Device Description
The Subject device is a light-cured methacrylate-based resin used in 3D printers for the production of temporary dental restorations. The Subject device is used by a dentist or dental technician for the CAD/CAM manufacturing of temporary dental restorations.
Restorations fabricated using the Subject device are one-time use, temporary, prescription-only devices. The Subject device is a viscous solution consisting of methacrylate-based resins, photo initiators and pigments.
Commonly used dental CAD software is used by dental professionals to virtually design a fixed indirect restoration and generate an industry-standard "STL" 3D dataset which reflects the intended shape and contour. The Subject resin is used within a validated manufacturing workflow to create the intended restoration. The Subject device is available in a variety of optional shades to reproduce the intended tooth shade of the restoration. Methacrylates are known materials, commonly used in the dental industry for fixed and removable prosthetic devices due to their physical-chemical, mechanical and biocompatible properties.
The Subject device is intended to be sold by the bottle and used with compatible hardware 3D printers and their nesting software, and post-curing devices.
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Not Found
Indicated Patient Age Range
Not Found
Intended User / Care Setting
dentist or dental technician
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)
Validation of the manufacturing process was performed demonstrating consistency of the process output with that of the process input and confirm compatibility with 3D Printers and Post-curing equipment. Assessment of printer compatibility was performed through evaluation of light output, printer resolution, and printer accuracy testing to internal protocols and confirmatory biocompatibility testing.
Physical material property testing was performed on the Subject device to ISO 10477:2018, Dentistry - Polymer-based crown and veneering materials. Results demonstrated the Subject device meets the property requirements of the referenced standard for; Depth of Cure, Flexural Strength, Water Solubility, Surface Finish, Shade Consistency and Color Stability.
A biological evaluation was performed on the Subject device. Biocompatibility testing was performed on the Subject device according to ISO 10993-1:2018 and ISO 7405:2014. Test included: Cytotoxicity, Irritation, Sensitization, Acute Systemic Toxicity, Material-mediated Pyrogenicity, Subacute Toxicity, Genotoxicity and Implantation.
Accelerated and Real-time Shelf life testing was performed to validate device packaging and material stability during storage.
Non-clinical performance testing of the Subject device met the acceptance criteria for each validation and test described above. This non-clinical performance testing demonstrates that the Subject device is suitable for intended use.
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
§ 872.3770 Temporary crown and bridge resin.
(a)
Identification. A temporary crown and bridge resin is a device composed of a material, such as polymethylmethacrylate, intended to make a temporary prosthesis, such as a crown or bridge, for use until a permanent restoration is fabricated.(b)
Classification. Class II.
0
Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health and Human Services logo. To the right of that is the FDA logo, which is a blue square with the letters "FDA" in white. To the right of the blue square is the text "U.S. FOOD & DRUG ADMINISTRATION" in blue.
January 14, 2022
Guangzhou Heygears Imc. Inc Chris Brown Manager Aclivi, LLC 3250 Brackley Drive Ann Arbor, Michigan 48105
Re: K213643
Trade/Device Name: UltraPrint-Dental Temp C&B UV Regulation Number: 21 CFR 872.3770 Regulation Name: Temporary Crown And Bridge Resin Regulatory Class: Class II Product Code: EBG Dated: November 16, 2021 Received: November 18, 2021
Dear Chris Brown:
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. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. 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.
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
1
801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
For Michael E. Adjodha, M.ChE. Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
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4. Indications for Use Statement
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Indications for Use
510(k) Number (if known)
Device Name UltraPrint-Dental Temp C&B UV
Indications for Use (Describe)
UltraPrint-Dental Temp C&B UV is indication of temporary dental restorations in conjunction with extra-oral curing light equipment. Duration is not more than 28 days in oral environment.
Type of Use (Select one or both, as applicable)
X Prescription Use (Part 21 CFR 801 Subpart D)
| Over-The-Counter Use (21 CFR 801 Subpart C)
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K213643 510(k) Summary GUANGZHOU HEYGEARS IMC.INC UltraPrint-Dental Temp C&B UV 12/30/2021
ADMINISTRATIVE INFORMATION
| Manufacturer Name | GUANGZHOU HEYGEARS IMC.INC |
|---|---|
| Block B2, 501, 601 | |
| Enterprise Accelerator, Kaifa District | |
| Guangzhou, Guangdong, 510700, China | |
| Telephone: +86-17612078809 | |
| Official Contact | Lin Liu - Registration Supervisor |
| hzhang5@heygears.com |
DEVICE NAME AND CLASSIFICATION
| Proprietary/Device Name: | UltraPrint-Dental Temp C&B UV |
|---|---|
| Common Name: | Crown and Bridge, Temporary, Resin |
| Regulation Description: | Temporary Crown And Bridge Resin |
| Regulation Number: | 21 CFR 872.3770 |
| Device Class: | Class II |
| Product Code: | EBG |
| Review Panel: | Dental |
| Reviewing Branch: | Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices (OHT1) |
| Dental Devices (DHT1B) |
PREDICATE DEVICE INFORMATION
The Subject device in this submission is substantially equivalent in indications, use and design principles to the following Predicate device.
| 510(k) | Predicate Device Name | Company Name |
|---|---|---|
| K200273 | FREEPRINT temp | DETAX GmbH & Co.KG |
INDICATIONS FOR USE
UltraPrint-Dental Temp C&B UV is indication of temporary dental restorations in conjunction with extra-oral curing light equipment. Duration is not more than 28 days in oral environment.
DEVICE DESCRIPTION
The Subject device is a light-cured methacrylate-based resin used in 3D printers for the production of temporary dental restorations. The Subject device is used by a dentist or dental technician for the CAD/CAM manufacturing of temporary dental restorations.
Restorations fabricated using the Subject device are one-time use, temporary, prescription-only devices. The Subject device is a viscous solution consisting of methacrylate-based resins, photo initiators and pigments.
Commonly used dental CAD software is used by dental professionals to virtually design a fixed indirect restoration and generate an industry-standard "STL" 3D dataset which reflects the intended shape and contour. The Subject
5
resin is used within a validated manufacturing workflow to create the intended restoration. The Subject device is available in a variety of optional shades to reproduce the intended tooth shade of the restoration. Methacrylates are known materials, commonly used in the dental industry for fixed and removable prosthetic devices due to their physical-chemical, mechanical and biocompatible properties.
The Subject device is intended to be sold by the bottle and used with compatible hardware 3D printers and their nesting software, and post-curing devices.
EQUIVALENCE TO MARKETED DEVICE
The Subject device is highly similar to the Primary Predicate device with respect to Indications for Use and technological principles. The comparison tables below compare the Indications for Use and Technological Characteristics of the Subject and Predicate devices.
Indications For Use
| Device | Indications for Use Statement |
|---|---|
| Subject Device | |
| UltraPrint-Dental Temp C&B UV | |
| GUANGZHOU HEYGEARS IMC.INC | UltraPrint-Dental Temp C&B UV is indicated for the fabrication of temporary dental restorations in |
| conjunction with extra-oral curing light equipment. Duration is not more than 28 days in oral | |
| environment. | |
| Predicate Device | |
| FREEPRINT temp (K200273) | |
| DETAX GmbH & Co.KG | FREEPRINT temp is indicated for the fabrication of temporary dental restorations in conjunction |
| with extra-oral curing light equipment. Duration is less than 30 days in oral environment. |
The Subject and Predicate Indications for Use Statement (IFUS) are highly similar, differing only by the device name and two days difference in duration. Slight differences in the Indications for Use Statements does not change the intended use of the Subject and Reference device to fabricate temporary dental restorations.
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Technological Characteristics
| Parameter | Subject Device | Predicate Device | Comparison with
Predicate Device |
|-----------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------|
| | UltraPrint-Dental Temp C&B UV
GUANGZHOU HEYGEARS IMC.INC | FREEPRINT temp (K200273)
DETAX GmbH & Co.KG | |
| Product Code | EBG | EBG | Same |
| Regulation Number | 872.3770 | 872.3770 | Same |
| Regulatory Class | Class II | Class II | Same |
| Intended Use | UltraPrint-Dental Temp C&B UV is
indicated for the fabrication of
temporary dental restorations in
conjunction with extra-oral curing light
equipment. Duration is not more than
28 days in oral environment. | FREEPRINT temp is indicated for the
fabrication of temporary dental
restorations in conjunction with extra-
oral curing light equipment. Duration is
less than 30 days in oral environment. | Highly Similar |
| Technology | 3D liquid (light-cured) print resin for
dental CAD/CAM | 3D liquid (light-cured) print resin for
dental CAD/CAM | Same |
| Material | Methacrylate polymer resin
(includes dimethacrylate) | Methacrylate polymer resin
(dimethacrylate) | Highly Similar |
| Material Shades | Common VITA-shades | Common VITA-shades | Same |
| Biocompatible | Yes | Yes | Same |
| OTC or Rx | Rx | Rx | Same |
| Sterile | Non-sterile | Non-sterile | Same |
| Chemical Composition | Methacrylate polymer resin with photo
initiator, and pigments | (Meth)acrylate-based resin with photo
initiator and pigments | Highly Similar |
| Polymerization (Curing)
Method | Visible light, 385 nm
w/post curing | Visible light, 385 nm
w/post curing | Same |
| Equipment | Validated 3D-Printer and post curing
devices | Validated 3D-Printer and post curing
devices | Same |
| Performance Testing | ISO 10477:2018 | ISO 10477:2018 | Same |
| Biocompatibility Testing | ISO 7405:2018
ISO 10993-1:2018
ISO 10993-3:2014
ISO 10993-5:2009
ISO 10993-6:2016
ISO 10993-10:2013
ISO 10993-11:2017 | ISO 7405:2014
ISO 10993-1:2018
ISO 10993-3:2014
ISO 10993-5:2009
ISO 10993-10:2013
ISO 10993-11:2017 | Highly Similar |
The Technological Characteristics of the Subject and Predicate devices are the same or Highly Similar.
Material/Chemical Composition - The Subject and Predicate devices are same Highly Similar in they are both methacrylate polymer resins. Slight differences in chemical composition do not change the intended use of the Subject and Predicate devices to be used in the fabrication of temporary dental prostheses. The Subject device has demonstrated suitability for intended use through material non-clinical performance testing.
Technological differences between the Subject and Predicate devices have been evaluated through non-clinical performance testing. The results of the tests performed show that Subject device meets the requirements mentioned in the applicable standards and confirm that the device performs similarly to Predicate device.
CLINICAL TESTING
The performance of methacrylate-based polymer resins in the clinical environment has been well established. No clinical data is included in this submission.
NON-CLINICAL PERFORMANCE TESTING
Validation of the manufacturing process was performed demonstrating consistency of the process output with that of the process input and confirm compatibility with 3D Printers and Post-curing equipment. Assessment of printer compatibility was performed through evaluation of light output, printer resolution, and printer accuracy testing to internal protocols and confirmatory biocompatibility testing.
Physical material property testing was performed on the Subject device to ISO 10477:2018, Dentistry - Polymerbased crown and veneering materials. Results demonstrated the Subject device meets the property requirements
7
of the referenced standard for; Depth of Cure, Flexural Strength, Water Solubility, Surface Finish, Shade Consistency and Color Stability.
A biological evaluation was performed on the Subject device. Biocompatibility testing was performed on the Subject device according to ISO 10993-1:2018 and ISO 7405:2014. Test included: Cytotoxicity, Irritation, Sensitization, Acute Systemic Toxicity, Material-mediated Pyrogenicity, Subacute Toxicity, Genotoxicity and Implantation.
Accelerated and Real-time Shelf life testing was performed to validate device packaging and material stability during storage.
No animal testing data is included in this submission.
Non-clinical performance testing of the Subject device met the acceptance criteria for each validation and test described above. This non-clinical performance testing demonstrates that the Subject device is suitable for intended use.
CONCLUSION
Overall, the Indications for Use statements for the Subject and Predicate devices are highly similar differing only in device name and slightly in use duration. Overall, the Technological Characteristics of the Subject device are the same or highly similar to the Predicate device with any differences mitigated through nonclinical performance testing.
Overall, these similarities between the Subject and Predicate devices, support a determination of substantial equivalence.