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Proactive You 1.0.3

by Virtusense Technologies, Inc.

Proactive You 1.0.3 is a Class II device made by Virtusense Technologies, Inc., listed in FDA GUDID since 1 Dec 2025 (UDI-DI 00860011881728), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860011881728 UDI-DI Date1 Dec 2025ListedStatusListed 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  • Withdrawn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
Proactive You
Generic name
Virtual-display rehabilitation system, non-supportive, clinical
Model / reference
1.0.3
Primary DI / UDI-DI
00860011881728
FDA product code
QKC
GMDN term
Virtual-display rehabilitation system, non-supportive, clinical
Device class
Class II
Regulation number
890.5360
GUDID distribution status
In Commercial Distribution

Other devices from Virtusense Technologies, Inc.

Properties

  • Prescription use
  • Premarket exempt
Other properties (13, all answered No)