N2
K-Number: K240754 · 2024-03-21
Device Summary
Frequently Asked Questions
What is the N2?
N2 is a medical device that received FDA 510(k) clearance on 2024-03-21. The listed applicant is Megagen Implant Co., Ltd.. The 510(k) number is K240754.
When did N2 receive FDA 510(k) clearance?
N2 received FDA 510(k) clearance on 2024-03-21, under 510(k) number K240754.
Who is the listed applicant for N2?
The FDA 510(k) record lists Megagen Implant Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for N2?
The FDA product code for N2 is EIA.
Other records listing Megagen Implant 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: EIA)
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.