(211 days)
No
The summary describes a physical dental abutment and its intended use, manufacturing process, and performance testing. There is no mention of software, algorithms, or any technology that would typically incorporate AI or ML. The "Mentions AI, DNN, or ML" field is explicitly marked as "Not Found".
No
This device is an abutment for dental implants, supporting prostheses. It replaces missing body parts and improves function rather than treating or preventing disease or affecting the structure or function of the body for therapeutic purposes.
No
This device, s-Clean Pre-Milled Abutment Mini, is described as a support for dental prostheses, used for fabricating patient-specific abutments. Its function is to structurally support restorations, not to diagnose a medical condition or disease.
No
The device description explicitly states it is a "Patient-specific abutment is made from titanium alloy" and mentions physical components like "diameters" and "connection designs," indicating it is a physical medical device, not software-only.
Based on the provided information, this device is not an IVD (In Vitro Diagnostic).
Here's why:
- Intended Use: The intended use is to support dental prostheses in the maxilla or mandible of a patient. This is a direct clinical application within the body, not a test performed on samples taken from the body.
- Device Description: The device is a physical abutment made of titanium alloy, designed to be implanted and used as a structural support.
- Lack of IVD Characteristics: There is no mention of the device being used to examine specimens (like blood, urine, tissue, etc.) to provide information for diagnosis, monitoring, or screening. The device itself is the treatment component, not a diagnostic tool.
Therefore, the s-Clean Pre-Milled Abutment Mini is a medical device used in dentistry, but it does not fit the definition of an In Vitro Diagnostic device.
N/A
Intended Use / Indications for Use
s-Clean Pre-Milled Abutment Mini is intended for use with dental implants as a support for single or multiple tooth prostheses in the maxilla or mandible of a partially or fully edentulous patient.
All digitally designed abutments for use with s-Clean Pre-Milled Abutment Mini are intended to be manufactured at a Dentis validated milling center.
Product codes
NHA
Device Description
Patient-specific abutment is made from titanium alloy conforming to ASTM F136 titanium abutment to be used in fabricating patient-specific abutments. The subject abutments are indicated for cemented or "Screw-and Cement-Retained Prosthesis(SCRP)" restorations. Each patient-specific abutment is individually prescribed by the clinician.
The diameters of patient-specific abutment are 5.8, 6.8mm and two connection designs (Hex, Non-hex).
Patient-Specific Abutment is compatible with following Implant Systems:
Proprietary Name: Dentis s-Clean s-Line Mini
Compatible Implants (K number): K210080
Implant diameter size: 5.8/6.8
Implant Interface Connection Type/Size (mm): Internal Connection type / 2.1
Type of Implant-Abutment Connection: Hex/Non-Hex
s-Clean Pre-Milled Abutment Mini are supplied with s-Clean abutment screw Mini, previously cleared in K210080 and provided non-sterile.
Materials:
- s-Clean Pre-Milled Abutment Mini and s-Clean Abutment Screw s-Line Mini is fabricated from Ti-6Al-4V ELI (Conforming to ASTM Standard F136).
Mentions image processing
Not Found
Mentions AI, DNN, or ML
Not Found
Input Imaging Modality
Not Found
Anatomical Site
Oral Cavity
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: Non-Clinical Testing
Sample Size: Not specified, but involved worst-case scenario testing.
Key Results: The subject device was tested to evaluate its substantial equivalence according to ISO 14801:2016 for fatigue. Biocompatibility testing according to ISO 10993-1:2009 and End User Sterilization Validation Test Report according to ANSI/AAMI ST79, ISO 17665-1, ISO 17665-2, ISO 11737-1, ISO 11737-2, and ISO 11138-1 were leveraged from previously cleared devices (K200099, K111364).
The results have met the criteria of the standards and demonstrated substantial equivalence with the predicate device. Clinical testing was not necessary to establish substantial equivalency.
Key Metrics
Not Found
Predicate Device(s)
Reference Device(s)
Predetermined Change Control Plan (PCCP) - All Relevant Information
Not Found
§ 872.3630 Endosseous dental implant abutment.
(a)
Identification. An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation.(b)
Classification. Class II (special controls). The guidance document entitled “Class II Special Controls Guidance Document: Root-Form Endosseous Dental Implants and Endosseous Dental Implant Abutments” will serve as the special control. (See § 872.1(e) for the availability of this guidance document.)
0
Image /page/0/Picture/0 description: The image contains the logos of the Department of Health & Human Services and the Food and Drug Administration (FDA). The Department of Health & Human Services logo is on the left, and the FDA logo is on the right. The FDA logo includes the letters "FDA" in a blue square, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue text.
Dentis Co., Ltd. % April Lee Consultant Withus Group Inc 106 Superior Irvine, California 92620
Re: K210410
Trade/Device Name: s-Clean Pre-Milled Abutment Mini Regulation Number: 21 CFR 872.3630 Regulation Name: Endosseous Dental Implant Abutment Regulatory Class: Class II Product Code: NHA Dated: June 10, 2021 Received: June 15, 2021
Dear April Lee:
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.
1
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 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 medical devices and radiation-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.
Andrew I. Steen Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health
Enclosure
2
Indications for Use
510(k) Number (if known) K210410
Device Name s-Clean Pre-Milled Abutment Mini
Indications for Use (Describe)
s-Clean Pre-Milled Abutment Mini is intended for use with dental implants as a support for single or multiple tooth prostheses in the maxilla or mandible of a partially or fully edentulous patient.
All digitally designed abutments for use with s-Clean Pre-Milled Abutment Mini are intended to be manufactured at a Dentis validated milling center.
| Type of Use (Select one or both, as applicable) |
|---|
| ☑ Prescription Use (Part 21 CFR 801 Subpart D) |
| ☐ Over-The-Counter Use (21 CFR 801 Subpart C) |
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3
510(k) Summary
Submitter
Dentis Co., Ltd. Gyu Ri Kim 99, Seongseoseo-ro, Dalseo-gu Daegu, 42718 Korea Email: kgr1026@dentis.co.kr Tel. +82-53-589-3541 Fax. +82-53-289-7922
Device Information
● Trade Name: s-Clean Pre-Milled Abutment Mini
- Common Name: Dental Abutment System
- Classification Name: Endosseous dental implant abutment
- Product Code: NHA
- Panel: Dental
- Regulation Number: 872.3630
- Device Class: Class II ●
- . Date prepared: 09/09/2021
Predicate Devices:
Primary Predicate K181037, DIO CAD/CAM Abutment by DIO CORPORATION
Reference Device K200099, s-Clean SQ-SL Implant System Mini by Dentis Co., Ltd. K111364, Haptite Coating Implant System by Dentis Co., Ltd.
Indications for Use:
s-Clean Pre-Milled Abutment Mini is intended for use with dental implants as a support for single or multiple tooth prostheses in the maxilla or mandible of a partially or fully edentulous patient.
All digitally designed abutments for use with s-Clean Pre-Milled Abutment Mini are intended to be manufactured at a Dentis validated milling center.
Official Correspondent
Withus Group Inc. April Lee 106 Superior, Irvine, CA 92620 USA Email: withus6664@gmail.com Phone: 1-909-274-9971 Fax: 1-909-460-8122
4
Device Description:
Patient-specific abutment is made from titanium alloy conforming to ASTM F136 titanium abutment to be used in fabricating patient-specific abutments. The subject abutments are indicated for cemented or "Screw-and Cement-Retained Prosthesis(SCRP)" restorations. Each patient-specific abutment is individually prescribed by the clinician.
The diameters of patient-specific abutment are 5.8, 6.8mm and two connection designs (Hex, Non-hex).
Patient-Specific Abutment is compatible with following Implant Systems:
| Proprietary Name | Dentis s-Clean s-Line Mini |
|---|---|
| Compatible Implants (K number) | K210080 |
| Implant diameter size | 5.8/6.8 |
| Implant Interface Connection Type/Size (mm) | Internal Connection type / 2.1 |
| Type of Implant-Abutment Connection | Hex/Non-Hex |
s-Clean Pre-Milled Abutment Mini are supplied with s-Clean abutment screw Mini, previously cleared in K210080 and provided non-sterile.
Materials:
- . s-Clean Pre-Milled Abutment Mini and s-Clean Abutment Screw s-Line Mini is fabricated from Ti-6Al-4V ELI (Conforming to ASTM Standard F136).
5
Summaries of Technology Characteristics
The subject device is substantially equivalent to the current cleared devices. They are substantially equivalent in intended use, material and connection interfaces to the implants are identical diameter and connection type. Comparison demonstrating Substantial Equivalence follows:
| Subject Device | Primary Predicate Device | |||
|---|---|---|---|---|
| Applicant | Dentis Co., Ltd. | DIO Corporation | ||
| Trade Name | s-Clean Pre-Milled Abutment Mini | DIO CAM/CAM Abutment | ||
| 510(k) No. | Not yet assigned | K181037 | ||
| Classification Name | Endosseous Dental Implant, Abutment (872.3630) | Endosseous Dental Implant, Abutment (872.3630) | ||
| Product Code | NHA | NHA | ||
| Class | II | II | ||
| Material | Ti-6AL-4V ELI (ASTM F136) | Ti-6AL-4V ELI (ASTM F136) | ||
| Diameter (mm) | CAD/CAM Patient-Specific Abutment | |||
| : 5.8/6.8 | CAD/CAM Patient-Specific Abutment | |||
| : 3.0/3.3/3.8/4.0/4.5/5.0/5.5/6.0/6.5/7.0 | ||||
| Sterile | Steam Sterilization by user | |||
| (Provided Non-Sterile) | Steam Sterilization by user | |||
| (Provided Non-Sterile) | ||||
| Type of Retention | Screw-retained or cement retained | Screw-retained or cement retained | ||
| Abutment Seat | Sits on Taper | Sits on Taper | ||
| Anatomical Site | Oral Cavity | Oral Cavity | ||
| Constructions | Machined | Machined | ||
| s-Clean Pre-Milled Abutment Mini is intended for use with dental | ||||
| implants as a support for single or multiple tooth prostheses in the maxilla | ||||
| or mandible of a partially or fully edentulous patient. | DIO CAD/CAM Abutment is intended for use with dental implants as a | |||
| support for single or multiple tooth prostheses in the maxilla or mandible of | ||||
| a partially or fully edentulous patient. | ||||
| Indications For Use/ | ||||
| Intended Use | All digitally designed abutments for use with s-Clean Pre-Milled | |||
| Abutment Mini are intended to be manufactured at a Dentis validated | ||||
| milling center. | Implant System | |||
| Compatibility | Implant Diameter | |||
| (mm) | ||||
| UF(II) Narrow | ||||
| Implant System | 3.0/3.3 | |||
| UF Sub merged | ||||
| Implant System | 3.8/4.0/4.5/5.0/5.5/ | |||
| 6.0/6.5/7.0 | ||||
| Platform Diameter | ||||
| (mm) | ||||
| 3.0/3.3 | ||||
| 3.8/4.0/4.5/5.0/5.5/ | ||||
| 6.0/6.5/7.0 |
6
| | | UF(II) Implant
System | | 3.8/4.0/4.5/5.0/5.5 | 3.8/4.0/4.5/5.0/5.5 |
|------------------------------------------|--|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--|---------------------|---------------------|
| | | Patient specific abutment is intended for use with the UF implant systems
provided in the chart. All digitally designed abutments for use with DIO
CAD/CAM Abutments are intended to be manufactured at a DIO
Corporation validated milling center. | | | |
| Substantial
Equivalence
Comparison | | The subject patient specific abutment is substantially equivalent in designs, dimensions, material, indications, abutment seat, screw seat,
anatomical site, connection, and technological characteristics with the identified primary predicate device. The patient specific abutment
is similar in fundamental scientific technology to the predicate.
The Indications for Use of the subject and primary predicate device are identical other than the compatible implant bodies. This
difference is mitigated by fatigue testing, and identification of reference device for compatible implant bodies. Both the predicate and
subject devices are intended to be milled into patient specific abutments using CAD/CAM technology under the manufacturing control
of the sponsor. Any differences in technology characteristics are accompanied by information that demonstrated the device is
substantially equivalent as the predicate. | | | |
7
Non-Clinical Testing
The subject device was tested to evaluate its substantial equivalence according to the following standards.
-
Fatigue Tests on subject device under the worst-case scenario according to ISO 14801:2016 .
Below tests were performed for predicate devices and leveraged for the subject device: -
Biocompatibility testing according to ISO 10993-1:2009 abutments referenced in K200099 ●
-
. End User Sterilization Validation Test Report according to ANSI/AAMI ST79, ISO 17665-1, ISO 17665-2, ISO 11737-1, ISO 11737-2, and ISO 11138-1 referenced in K111364 A worst-case evaluation showed that the previously cleared device was able to be leveraged for the steam sterilization of the subject device
The results of the above tests have met the criteria of the standards and demonstrated the substantial equivalence with the predicate device.
Non-clinical test data was conducted in accordance with the recommendations of FDA Guidance "Class II Special Controls Guidance Document: Root-form Endosseous Dental Implants and Endosseous Dental Implant Abutments", and it consisted of testing finished assembled implant/abutment systems of the worstcase scenario, (smallest diameter with maximum angulation) through fatigue testing.
Clinical testing was not necessary to establish substantial equivalency of the device.
Conclusion
The s-Clean Pre-Milled Abutment Mini constitutes a substantially equivalent medical device, meeting all the declared requirements of its intended use. This system has the same intended use and fundamental scientific technology as its predicate devices. Therefore, the s-Clean Pre-Milled Abutment Mini and its predicates are substantially equivalent.