Cercon® yo ML
K-Number: K241557 · 2024-08-28
ApplicantDentsply Sirona
Decision Date2024-08-28
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Cercon® yo ML is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2024-08-28 under approval number K241557. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Cercon® yo ML?
Cercon® yo ML is a medical device that received FDA 510(k) clearance on 2024-08-28. It is manufactured by Dentsply Sirona. The 510(k) number is K241557.
When was Cercon® yo ML approved by the FDA?
Cercon® yo ML received FDA 510(k) clearance on 2024-08-28, under approval number K241557.
What company makes Cercon® yo ML?
Cercon® yo ML is manufactured by Dentsply Sirona.
What is the FDA product code for Cercon® yo ML?
The FDA product code for Cercon® yo ML is EIH.
Other Devices by Dentsply Sirona
Related Devices (Code: EIH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.