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Neuro Touch SDNTST0123US

by Yostra Labs Private Limited

Neuro Touch SDNTST0123US is a vibratory biothesiometer (FDA Class I) made by Yostra Labs Private Limited, listed in FDA GUDID since 10 Jan 2024 (UDI-DI 08908022363016), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08908022363016 UDI-DI Date10 Jan 2024ListedStatusListed 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  • Withdrawn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
Neuro Touch
Generic name
Vibratory biothesiometer
Model / reference
SDNTST0123US
Primary DI / UDI-DI
08908022363016
FDA product code
GXB, LLN, LQW
GMDN term
Vibratory biothesiometer
Device class
Class I
Regulation number
882.1500, 882.1200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Thermotester, diagnosticVibratory biothesiometerPressure algometer/aesthesiometer, electronic

Similar devices

Other devices filed under FDA product code GXB (Esthesiometer).

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)