Endosolv
by Septodont
510(k) K172839
Endosolv is a medical device (FDA Class II; FDA product code KIF, Resin, Root Canal Filling) made by Septodont, cleared under FDA 510(k) K172839 on 13 Feb 2018, active as of 22 Oct 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 | NumberK172839 | Date13 Feb 2018 | StatusActive |
Official records
- FDA 510(k) database K172839
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- Withdrawn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
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