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LimFlow Vector

FDA UDIFDA 510(k)

Class II (US FDA UDI)

510(k) K260188

by Limflow Inc.

Identity

Trade Name
LimFlow Vector FDA UDI
Generic Name
Valvulotome, percutaneous FDA UDI
Device Name
The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves FDA UDI
Model / Reference
VT-US-21 FDA UDI
Description
The LimFlow Vector is intended for the treatment of vascular disorders and more particularly for excising or disrupting venous valves FDA UDI

Identifiers

Primary DI / UDI-DI
00850041730028 FDA UDI
FDA Product Code
MGZ FDA UDI
GMDN Term
Valvulotome, percutaneous FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4885 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Valvulotome, percutaneous

LimFlow Vector by Limflow Inc. — Class II — FDA_510K — listed in FDA GUDID, FDA 510(k) — regulatory data on deviCERTS

Similar devices

Also classified as Valvulotome, percutaneous.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

United States Active

FDA_510K

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Manufacturer

Manufacturer
Limflow Inc.
FDA Applicant
LimFlow, Inc.

Sources (2)

  • FDA UDI 101909d6-49d4-4d01-9cc6-96ba486e9467 58 fields · synced Jun 19, 2026
  • FDA 510(k) K260188 1 fields · synced Jun 4, 2026