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Golden Technologies, Inc.

United StatesFDA applicant, unverified

Devices
8
FDA recalls
2

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

Catalogue8

Newest first, rows 1-8 of 8

  • Golden Hawk Ref K971050

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Companion Model 221, 321, 421 Ref K012258

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Golden Eagle Ref K971043

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Alante, Battery Operated Power Wheelchair Ref K011153

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Buzzaround, Vehicle, Motorized 3-Wheeled Ref K041025

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Golden Spyder, Model Gs-300 Ref K041341

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Golden Power Lift Chair Ref K880800

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Golden Liteway Ref K063162

    Active Regimes: 510(k) Registry: 510(k) Class:II

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 1
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0

1 initiated before 2017

  • 2020

    • 6 Jul 2020 Z-2817-2020 Class II Terminated Suspect poor weld on back KD bar. Distribution: US Only Submission number: K880800
  • 2014

    • 21 Jan 2014 Z-1235-2014 Class II Terminated Buzzaround XL scooters' front to rear lockup can become unintentionally disengaged due to possible improper fit of the front alignment cup to the rear alignment screw. Distribution: Worldwide Distribution - USA Nationwide Submission number: K041025

Frequently asked questions

How many devices does Golden Technologies, Inc. have in the registry?

The registry currently lists 8 devices for Golden Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Golden Technologies, Inc.'s devices?

Among its 8 most recently registered devices, Golden Technologies, Inc. has devices listed in FDA 510(k) (8 devices).

What risk classes do Golden Technologies, Inc.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for Golden Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Golden Technologies, Inc.?

FDA recall records list 2 recalls initiated by Golden Technologies, Inc., the most recent initiated on 2020-07-06. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Golden Technologies, Inc. in the registry?

The most recently registered devices listed for Golden Technologies, Inc. include GOLDEN HAWK, COMPANION MODEL 221, 321, 421, GOLDEN EAGLE and ALANTE, BATTERY OPERATED POWER WHEELCHAIR.

Generated automatically from registry data and not verified by a human reviewer.