3D Endo Software
K-Number: K171115 · 2017-07-17
ApplicantDentsply Sirona
Decision Date2017-07-17
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
3D Endo Software is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2017-07-17 under approval number K171115. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the 3D Endo Software?
3D Endo Software is a medical device that received FDA 510(k) clearance on 2017-07-17. It is manufactured by Dentsply Sirona. The 510(k) number is K171115.
When was 3D Endo Software approved by the FDA?
3D Endo Software received FDA 510(k) clearance on 2017-07-17, under approval number K171115.
What company makes 3D Endo Software?
3D Endo Software is manufactured by Dentsply Sirona.
What is the FDA product code for 3D Endo Software?
The FDA product code for 3D Endo Software is LLZ.
Other Devices by Dentsply Sirona
Related Devices (Code: LLZ)
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.