Any-Core
FDA 510(k) K252465 · Mediclus Co., Ltd.
510(k) numberK252465
Submission
- Device name
- Any-Core
- Applicant
- Mediclus Co., Ltd.
Cheongju-Si, KR - Received
- August 6, 2025
- Decision date
- December 5, 2025
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code EBF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262202 | Cerasmart ForteEBF · Traditional | GC America, Inc. | 09/10/2026SE |
| K261695 | Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)EBF · Traditional | Guilin Kevin Peter Technology Co., Ltd. | 08/31/2026SE |
| K262228 | Transcend Bulk Fill Flowable CompositeEBF · Traditional | Ultradent Products, Inc. | 07/01/2026SE |
| K261485 | Tetric plus Fill;Tetric plus FlowEBF · Traditional | Ivoclar Vivadent, Inc. | 07/01/2026SE |
| K261246 | SRGC-06EBF · Traditional | GC America, Inc. | 06/18/2026SE |
| K261093 | DiafilEBF · Traditional | DiaDent Group International | 06/02/2026SE |
| K261071 | DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW…EBF · Traditional | DiaDent Group International | 05/19/2026SE |
| K260805 | Dual CoreEBF · Traditional | Vericom Co., Ltd. | 05/11/2026SE |
| K261357 | Grandio disc multicolorEBF · Traditional | Voco GmbH | 04/27/2026SE |
| K261356 | Dura-CrownEBF · Special | Hangzhou SHINING3D Dental Technology Co., Ltd. | 04/27/2026SE |
More from Hangzhou SHINING3D Dental Technology Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K262074 | Any-ZircosEIH · Traditional | 08/21/2026SE |
| K254201 | Any-CemEMA · Traditional | 08/13/2026SE |
| K261728 | One-Fil LCEJK · Traditional | 07/21/2026SE |
| K260485 | Any-EtchKLE · Traditional | 05/14/2026SE |
| K260819 | Any-Com SealEBC · Traditional | 05/01/2026SE |
| K253797 | One-StopMVL · Traditional | 02/27/2026SE |
| K253167 | Any-PasteKIF · Traditional | 01/12/2026SE |
| K251884 | One-Fil Putty InjectableKIF · Special | 08/22/2025SE |
| K251283 | Once-Fil FlowEBF · Traditional | 06/06/2025SE |
| K250823 | Any-Com FlowEBF · Special | 04/14/2025SE |
Questions and answers
When was Any-Core cleared by the FDA?
Any-Core (K252465) received a 510(k) decision of Substantially Equivalent on December 5, 2025, 121 days after the submission was received.
What is the product code of K252465?
The FDA product code is EBF – Material, Tooth Shade, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3690.