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Stent LEV3528-PMA

by Microvention Inc.

Stent LEV3528-PMA is a Class III device made by Microvention Inc., listed in FDA GUDID since 26 Apr 2023 (UDI-DI 00842429117842), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842429117842 UDI-DI Date26 Apr 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Stent
Generic name
Bare-metal intracranial vascular stent
Model / Ref / Catalog
LEV3528-PMA, LEV3528
Primary DI / UDI-DI
00842429117842
FDA product code
QCA
GMDN term
Bare-metal intracranial vascular stent
Device class
Class III
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Bare-metal intracranial vascular stent

Other devices from Microvention Inc.

See all devices from Microvention Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)