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VSA 2 Handheld device

by Medoc Corp.

VSA 2 Handheld device (AS 00422) is a vibratory biothesiometer (FDA Class I; FDA product code IRO, Vibrator, Therapeutic) made by Medoc Corp., listed in FDA GUDID since 20 Jun 2023 (UDI-DI 07290103039660), 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 Number07290103039660 UDI-DI Date20 Jun 2023ListedStatusListed 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  • Withdrawn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

Generic name
Vibratory biothesiometer
Model / Ref / Catalog
VSA 2 Handheld Device, AS 00422
Primary DI / UDI-DI
07290103039660
FDA product code
IRO
GMDN term
Vibratory biothesiometer
Device class
Class I
Regulation number
890.5975
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vibratory biothesiometer

Similar devices

Other devices filed under FDA product code IRO (Vibrator, Therapeutic).

Other devices from Medoc Corp.

See all devices from Medoc Corp. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)