AEON Endoscopic Stapler
K-Number: K201882 · 2020-10-09
Device Summary
Frequently Asked Questions
What is the AEON Endoscopic Stapler?
AEON Endoscopic Stapler is a medical device that received FDA 510(k) clearance on 2020-10-09. The listed applicant is Lexington Medical, Inc.. The 510(k) number is K201882.
When did AEON Endoscopic Stapler receive FDA 510(k) clearance?
AEON Endoscopic Stapler received FDA 510(k) clearance on 2020-10-09, under 510(k) number K201882.
Who is the listed applicant for AEON Endoscopic Stapler?
The FDA 510(k) record lists Lexington Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AEON Endoscopic Stapler?
The FDA product code for AEON Endoscopic Stapler is GDW.
Other records listing Lexington Medical, Inc. 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: GDW)
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.