Medical Depot
Country not established
- Devices
- 4
- FDA recalls
- 93 ongoing
At a glance
Market reach
- United States
- FDA recalls
What Medical Depot makes
Medical Depot manufactures the DRIVE SOLSTICE oxygen concentrator, a portable device designed to deliver concentrated oxygen for patients requiring supplemental oxygen therapy at home or on the move.
The DRIVE SOLSTICE oxygen concentrator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Medical Depot Power Neb 1 Ref K012006
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Medical Depot Nebulizer, Model Power Neb 2 Ref K003344
Regimes: 510(k) Registry: 510(k)Drive Solstice Oxygen Concentrator Ref K080391
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 9 recalls initiated by Medical Depot, the earliest on 2016-02-17 and the most recent on 2025-04-11. By recorded status: 3 ongoing and 6 terminated. The reasons filed fall into these groups: electrical or power and mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 2
- 2025 1
- 2026 0
2025
- 11 Apr 2025 Z-1727-2025 Class I Ongoing Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
Full distribution text
- 11 Apr 2025 Z-1727-2025 Class I Ongoing Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
2024
- 14 Jun 2024 Z-2354-2024 Class II Ongoing The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
- 14 Jun 2024 Z-2355-2024 Class II Ongoing The tiller separates from the base/front caster assembly. If the knee walker fails, a user may fall and sustain an injury
2016
- 17 Feb 2016 Z-2101-2016 Class II Terminated Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
- 17 Feb 2016 Z-2102-2016 Class II Terminated Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
- 17 Feb 2016 Z-2103-2016 Class II Terminated Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
- 17 Feb 2016 Z-2104-2016 Class II Terminated Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
- 17 Feb 2016 Z-2105-2016 Class II Terminated Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
- 17 Feb 2016 Z-2106-2016 Class II Terminated Tip crutch failure involving the bottom of the metal portion which comes in contact with ground
Frequently asked questions
How many devices does Medical Depot have in the registry?
The registry currently lists 4 devices for Medical Depot. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Depot's devices?
Among its 4 most recently registered devices, Medical Depot has devices listed in FDA 510(k) (4 devices).
What risk classes do Medical Depot's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medical Depot's devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Medical Depot?
FDA recall records list 9 recalls initiated by Medical Depot, the most recent initiated on 2025-04-11. 3 of them are recorded as ongoing. 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 Medical Depot in the registry?
The most recently registered devices listed for Medical Depot include MEDICAL DEPOT POWER NEB 1, MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA, ASTAIRE AND VIPER, MEDICAL DEPOT NEBULIZER, MODEL POWER NEB 2 and DRIVE SOLSTICE OXYGEN CONCENTRATOR.