510(k) K211995
K211995 is an FDA 510(k) premarket notification submitted by Sonendo, Inc. for the device "Sonendo Filling Material 5C". The FDA issued a decision of Substantially Equivalent on August 27, 2021. The device falls under product code KIF (Resin, Root Canal Filling), a Class II device regulated under 21 CFR 872.3820. Sonendo, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 27, 2021
- Date Received
- June 28, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Resin, Root Canal Filling
- Device Class
- Class II
- Regulation Number
- 872.3820
- Review Panel
- DE
- Submission Type