LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated
K-Number: K261070 · 2026-09-15
Device Summary
Frequently Asked Questions
What is the LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated?
LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated is a medical device that received FDA 510(k) clearance on 2026-09-15. The listed applicant is Covidien, LLC. The 510(k) number is K261070.
When did LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated receive FDA 510(k) clearance?
LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated received FDA 510(k) clearance on 2026-09-15, under 510(k) number K261070.
Who is the listed applicant for LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated?
The FDA 510(k) record lists Covidien, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated?
The FDA product code for LigaSure™ RAS Maryland Jaw Vessel Sealer/Divider, Nano-coated is GEI.
Other records listing Covidien, LLC 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: GEI)
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.