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Neuroblade System NB-20-110

by Clearmind Biomedical 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 Number00860000321389 UDI-DI Date11 May 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  • Withdrawn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
Neuroblade System
Generic Name
Surgical irrigation/aspiration cannula, illuminating, single-use
Model / Reference
NB-20-110
Primary DI / UDI-DI
00860000321389
510(k) Number
FDA Product Code
GWG, GEI
GMDN Term
Surgical irrigation/aspiration cannula, illuminating, single-use
Device Class
Class II
Regulation Number
882.1480, 878.4400
GUDID distribution status
In Commercial Distribution

Other devices from Clearmind Biomedical Inc.

Properties

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

Other properties (9)

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