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Lvis 212716-Lvis

by Microvention Inc.

Lvis 212716-Lvis is a device classified as Unclassified made by Microvention Inc., listed under FDA HDE H130005 and listed in FDA GUDID since 25 Nov 2018 (UDI-DI 00810170016288), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

HDE

Valid until

No date given

No validity date on record

FDA recalls

None found

in data synced 22 Oct 2026

Documents

HDE H130005

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810170016288 UDI-DI Date25 Nov 2018ListedStatusListed GUDID: in commercial distribution
United StatesFDA HDE from GUDID NumberH130005 Date—StatusActive

Official records

Across registries

2 registries list this device

  • FDA HDE H130005 Active
  • FDA GUDID UDI-DI 00810170016288 listed 25 Nov 2018 Listed

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA HDE Active

Specification

GUDID

Trade name
Lvis
Generic name
Bare-metal intracranial vascular stent
Model / Ref / Catalog
212716-LVIS
Primary DI / UDI-DI
00810170016288
PMA number
FDA product code
NJE
GMDN term
Bare-metal intracranial vascular stent
Device class
Unclassified
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Bare-metal intracranial vascular stent

Cleared under the same submission (H130005)

and 8 more cleared under H130005

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)