Data / Medical devices / South Korea / Snucone Co., Ltd.
Snucone Co., Ltd.: FDA-registered device maker in Dalseo-gu Daegu, South Korea, 2 510(k) clearances
Snucone Co., Ltd. is registered with the FDA (registration 3024858450) in Dalseo-gu Daegu, South Korea. It lists 4 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 8, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3024858450
- Address
- 5 Seongseo-ro 75-gil, Dalseo-gu Daegu, South Korea, 42703
- Owner or operator
- SNUCONE Co., LTD. (10086275)
- Roles
- Manufacturer
- First device listed
- October 26, 2022
- Registered through
- 2026
- Brand names listed
- ABIDING COUPLE DIGITAL LAB ANALOG, ABIDING COUPLE LAB ANALOG, ABIDING DIGITAL LAB ANALOG SCREW, ABIDING KIT, ABIDING MU LAB ANALOG, ABIDING MU SCANBODY, AF/EF COMPLETE KIT, AF/EF SNUCONE KIT and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Accessories, Implant, Dental, Endosseous | NDP | 1 | Manufacturer | accessdata.fda.gov |
| Drill, Dental, Intraoral | DZA | 1 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 8, 2023 | K222792 | SNUCONE Tissue Level Implant System | DZE | Substantially Equivalent | Snucone Co., Ltd. | accessdata.fda.gov |
| July 13, 2022 | K210354 | SNUCONE Bone Level Implant System | DZE | Substantially Equivalent | Snucone Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Implant, Endosseous, Root-Form
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Accessories, Implant, Dental, Endosseous
- All makers of Drill, Dental, Intraoral
Updated June 8, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.