LigaMend
K-Number: K253695 · 2026-02-27
ApplicantRiverpoint Medical, LLC
Decision Date2026-02-27
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
LigaMend is a medical device manufactured by Riverpoint Medical, LLC. It received FDA 510(k) clearance on 2026-02-27 under approval number K253695. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LigaMend?
LigaMend is a medical device that received FDA 510(k) clearance on 2026-02-27. It is manufactured by Riverpoint Medical, LLC. The 510(k) number is K253695.
When was LigaMend approved by the FDA?
LigaMend received FDA 510(k) clearance on 2026-02-27, under approval number K253695.
What company makes LigaMend?
LigaMend is manufactured by Riverpoint Medical, LLC.
What is the FDA product code for LigaMend?
The FDA product code for LigaMend is MBI.
Other Devices by Riverpoint Medical, LLC
Related Devices (Code: MBI)
K163034SUTUREFIX Curved Suture AnchorSmith and Nephew, Inc.
K162198GFS UltimateParcus Medical, LLC
K162386KATOR Suture AnchorKator, LLC
K161033AFX Femoral Implant With InserterCayenne Medical, Inc.
K160996Dunamis Suture Anchor PEEK 3.0mm, 3.5mm, 4.5mm, 5.5mm, 6.5mmDunamis, LLC
K161001MILAGRO ADVANCE PEEK Interference ScrewMedos International SARL
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.