Laport
K-Number: K252985 · 2026-05-19
Device Summary
Frequently Asked Questions
What is the Laport?
Laport is a medical device that received FDA 510(k) clearance on 2026-05-19. The listed applicant is Sejong Medical Co., Ltd.. The 510(k) number is K252985.
When did Laport receive FDA 510(k) clearance?
Laport received FDA 510(k) clearance on 2026-05-19, under 510(k) number K252985.
Who is the listed applicant for Laport?
The FDA 510(k) record lists Sejong Medical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Laport?
The FDA product code for Laport is GCJ.
Other records listing Sejong Medical 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: GCJ)
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.