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Laguna Clot Retriever System

FDA UDI

Class II (US FDA UDI)

by Innova Vascular, Inc.

Identity

Trade Name
Laguna Clot Retriever System FDA UDI
Generic Name
Thrombectomy wire-net FDA UDI
Device Name
One (1) Laguna Clot Retriever System: Laguna Clot Retriever and Delivery Sheath FDA UDI
Model / Reference
LAGUNA14-001 FDA UDI
Description
One (1) Laguna Clot Retriever System: Laguna Clot Retriever and Delivery Sheath FDA UDI

Identifiers

Primary DI / UDI-DI
00850041053097 FDA UDI
FDA Product Code
QEW FDA UDI
KRA FDA UDI
GMDN Term
Thrombectomy wire-net FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 FDA UDI
870.1210 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

Yes

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: Thrombectomy wire-net

Laguna Clot Retriever System by Innova Vascular, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy wire-net.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innova Vascular, Inc.

Sources (1)

  • FDA UDI 432b800b-c344-41d2-91f2-01f1ae0a8512 33 fields · synced Jun 1, 2026