Magic UCLA Abutment System
K-Number: K202418 · 2020-12-03
Device Summary
Frequently Asked Questions
What is the Magic UCLA Abutment System?
Magic UCLA Abutment System is a medical device that received FDA 510(k) clearance on 2020-12-03. The listed applicant is Innobiosurg Co., Ltd.. The 510(k) number is K202418.
When did Magic UCLA Abutment System receive FDA 510(k) clearance?
Magic UCLA Abutment System received FDA 510(k) clearance on 2020-12-03, under 510(k) number K202418.
Who is the listed applicant for Magic UCLA Abutment System?
The FDA 510(k) record lists Innobiosurg Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Magic UCLA Abutment System?
The FDA product code for Magic UCLA Abutment System is NHA.
Other records listing Innobiosurg 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: NHA)
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.