Ez3D-i / E3
K-Number: K163539 · 2016-12-23
Device Summary
Frequently Asked Questions
What is the Ez3D-i / E3?
Ez3D-i / E3 is a medical device that received FDA 510(k) clearance on 2016-12-23. The listed applicant is Ewoosoft Co., Ltd.. The 510(k) number is K163539.
When did Ez3D-i / E3 receive FDA 510(k) clearance?
Ez3D-i / E3 received FDA 510(k) clearance on 2016-12-23, under 510(k) number K163539.
Who is the listed applicant for Ez3D-i / E3?
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 Ez3D-i / E3?
The FDA product code for Ez3D-i / E3 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.