Skip to content

NeVasc .070 Aspiration Catheter, 115 cm VC-070-115

by Vesalio, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850083646004 UDI-DI Date26 Mar 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
NeVasc .070 Aspiration Catheter, 115 cm
Generic Name
Thrombectomy suction catheter
Model / Ref / Catalog
VC-070-115
Primary DI / UDI-DI
00850083646004
510(k) Number
FDA Product Code
NRY
GMDN Term
Thrombectomy suction catheter
Device Class
Class II
Regulation Number
870.1250
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K251006)

Other devices from Vesalio, Inc.

See all devices from Vesalio, Inc. →

Properties

  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date

Other properties (10)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No