EzDent-i / E2 / Prora View
K-Number: K172364 · 2017-08-22
ApplicantEwoosoft Co., Ltd.
Decision Date2017-08-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
EzDent-i / E2 / Prora View is a medical device manufactured by Ewoosoft Co., Ltd.. It received FDA 510(k) clearance on 2017-08-22 under approval number K172364. 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 EzDent-i / E2 / Prora View?
EzDent-i / E2 / Prora View is a medical device that received FDA 510(k) clearance on 2017-08-22. It is manufactured by Ewoosoft Co., Ltd.. The 510(k) number is K172364.
When was EzDent-i / E2 / Prora View approved by the FDA?
EzDent-i / E2 / Prora View received FDA 510(k) clearance on 2017-08-22, under approval number K172364.
What company makes EzDent-i / E2 / Prora View?
EzDent-i / E2 / Prora View is manufactured by Ewoosoft Co., Ltd..
What is the FDA product code for EzDent-i / E2 / Prora View?
The FDA product code for EzDent-i / E2 / Prora View is LLZ.
Other Devices by Ewoosoft Co., Ltd.
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.