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V-Grip Detachment Controller VG900

by Microvention Inc.

V-Grip Detachment Controller VG900 (VG501) is a Class II device made by Microvention Inc., listed in FDA GUDID since 28 Aug 2025 (UDI-DI 00816777020116), 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 Number00816777020116 UDI-DI Date28 Aug 2025ListedStatusListed 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  • Withdrawn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
V-Grip Detachment Controller
Generic name
Vascular implant detacher, electronic, single-use
Model / Ref / Catalog
VG900, VG501
Primary DI / UDI-DI
00816777020116
FDA product code
HCG
GMDN term
Vascular implant detacher, electronic, single-use
Device class
Class II
Regulation number
882.5950
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Vascular implant detacher, electronic, single-use

Similar devices in this category

Other devices filed under Vascular implant detacher, electronic, single-use.

Other devices from Microvention Inc.

See all devices from Microvention Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)