Companion (221 +2 more) - 421

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K012258 ↗

FDA Product Code

INI

Models / Variants

221

321

421

Device Class

Class II

Regulation

21 CFR Part 890.3800

Advisory Committee

Physical Medicine

FDA Decision

SESE Substantially Equivalent

• Golden Hawk

  Class II

  FDA 510(k) K971050 Active Cleared 1 Aug 1997

• Golden Eagle

  Class II

  FDA 510(k) K971043 Active Cleared 1 Aug 1997

• Alante, Battery Operated Power Wheelchair

  Class II

  FDA 510(k) K011153 Active Cleared 29 May 2001

• Buzzaround, Vehicle, Motorized 3-Wheeled

  Class II

  FDA 510(k) K041025 Active Cleared 3 May 2004

• Golden Spyder, Model Gs-300

  Class II

  FDA 510(k) K041341 Active Cleared 3 Jun 2004

• Golden Power Lift Chair

  Class II

  FDA 510(k) K880800 Active Cleared 14 Mar 1988

See all devices from Golden Technologies, Inc. →