Any-Paste
510(k) K253167
Any-Paste is a medical device (FDA Class II; FDA product code KIF, Resin, Root Canal Filling) made by MEDICLUS Co., Ltd., cleared under FDA 510(k) K253167 on 12 Jan 2026, active as of 12 Nov 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK253167 | Date12 Jan 2026 | StatusActive |
Official records
- FDA 510(k) database K253167
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KIF
- Device class
- Class II
- Regulation
- 21 CFR Part 872.3820
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K253167
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| Any-Paste 505-1 | EC2501001 / 505-1 | 08809518341511 | Weight 2 g | On the market |
Similar devices
Other devices filed under FDA product code KIF (Resin, Root Canal Filling).
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- LEE ENDOFILL, ROOT CANAL FILLING RESIN by Lee Pharmaceuticals
- THE BI-DIRECTIONAL SPIRAL & EPOXY ROOT CANAL CEMENT SYSTEM by Mds
- CZ-S2000 by PARKELL, INC.
- IROOT FS by Innovative BioCeramix Inc.
- C-Root 2g by Beijing C-Root Dental Medical Devices Co., LTD.
- Sealapex tubes, Sealapex bulk package, Sealapex Xpress dual-barrel syringes by Sybron Dental Specialties, Inc.
- C-Root 1g by Beijing C-Root Dental Medical Devices Co., LTD.