EzDent-i / E2 / Prora View
K-Number: K172364 · 2017-08-22
Device Summary
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. The listed applicant is Ewoosoft Co., Ltd.. The 510(k) number is K172364.
When did EzDent-i / E2 / Prora View receive FDA 510(k) clearance?
EzDent-i / E2 / Prora View received FDA 510(k) clearance on 2017-08-22, under 510(k) number K172364.
Who is the listed applicant for EzDent-i / E2 / Prora View?
The FDA 510(k) record lists Ewoosoft Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
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 records listing Ewoosoft Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LLZ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.