IU Implant System
K-Number: K172345 · 2018-06-18
Device Summary
Frequently Asked Questions
What is the IU Implant System?
IU Implant System is a medical device that received FDA 510(k) clearance on 2018-06-18. The listed applicant is Warantec Co., Ltd.. The 510(k) number is K172345.
When did IU Implant System receive FDA 510(k) clearance?
IU Implant System received FDA 510(k) clearance on 2018-06-18, under 510(k) number K172345.
Who is the listed applicant for IU Implant System?
The FDA 510(k) record lists Warantec Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IU Implant System?
The FDA product code for IU Implant System is DZE.
Other records listing Warantec 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: DZE)
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.