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DPNCheck NC-030

by Impulse Medical Technologies, 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 Number00816022023657 UDI-DI Date9 Jan 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  • Withdrawn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
DPNCheck
Generic Name
Diagnostic peripheral nerve electrical stimulation system
Model / Reference
NC-030
Primary DI / UDI-DI
00816022023657
510(k) Number
FDA Product Code
JXE
GMDN Term
Diagnostic peripheral nerve electrical stimulation system
Device Class
Class II
Regulation Number
882.1550
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K041320)

Other devices from Impulse Medical Technologies, Inc.

See all devices from Impulse Medical Technologies, Inc. →

Properties

  • Serial Number
  • Manufacturing Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No