ClearanceBrief
Company ยท US

LimFlow, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2026. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (1 in 12 months)
1recalls (1 in 12 months)
1recalls that name a 510(k)

Product codes

CodeDeviceRecords
MGZValvulotome3
MMXDevice, Percutaneous Retrieval2
PDUCatheter For Crossing Total Occlusions2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 18, 2026K260188LimFlow Vector
LimFlow, Inc.
MGZ
May 31, 2025K251376LimFlow ARC
LimFlow, Inc.
PDU
Feb 14, 2025K242776LimFlow V-Ceiver
LimFlow, Inc.
MMX
Dec 21, 2022K221902LimFlow Vector
LimFlow, Inc.
MGZ
Aug 31, 2022K221541LimFlow ARC
LimFlow, Inc.
PDU
Aug 9, 2022K222083LimFlow V-Ceiver
LimFlow, Inc.
MMX

Latest recalls

DateFirm and productCodeLinked 510(k)
Jan 29, 2026LimFlow, Inc.
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Open, Classified
MGZK221902
Get alerts for these product codes