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Vector Elite VEC-1000

by Bioness Inc.

Vector Elite VEC-1000 is a Class I device made by Bioness Inc., listed in FDA GUDID since 7 Dec 2017 (UDI-DI 00815962020269), 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 Number00815962020269 UDI-DI Date7 Dec 2017ListedStatusListed 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  • Withdrawn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
Vector Elite
Generic name
Gait rehabilitation frame, electric
Model / reference
VEC-1000
Primary DI / UDI-DI
00815962020269
FDA product code
BXB
GMDN term
Gait rehabilitation frame, electric
Device class
Class I
Regulation number
890.5380
GUDID distribution status
In Commercial Distribution

Related devices

Category: Gait rehabilitation frame, electric

Other devices from Bioness Inc.

See all devices from Bioness Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)