510(k) K251701
K251701 is an FDA 510(k) premarket notification submitted by Dentalez, Inc., Stardental Division for the device "Star E900 Electric System". The FDA issued a decision of Substantially Equivalent on January 12, 2026. The device falls under product code EBW (Controller, Foot, Handpiece And Cord), a Class I device regulated under 21 CFR 872.4200. Dentalez, Inc., Stardental Division has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 12, 2026
- Date Received
- June 2, 2025
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Controller, Foot, Handpiece And Cord
- Device Class
- Class I
- Regulation Number
- 872.4200
- Review Panel
- DE
- Submission Type