Human Design Medical, LLC
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Z1 Cpap System Ref K140929
Regimes: 510(k) Registry: 510(k)
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 1
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2018
- 8 May 2018 Z-2530-2018 Class III Terminated Some Vivo 65 devices have an unreleased version of the Firmware upgrade tool.
Frequently asked questions
How many devices does Human Design Medical, LLC have in the registry?
The registry currently lists 1 device for Human Design Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Human Design Medical, LLC's devices?
Among its 1 most recently registered device, Human Design Medical, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Human Design Medical, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Human Design Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Human Design Medical, LLC?
FDA recall records list 1 recall initiated by Human Design Medical, LLC, the most recent initiated on 8 May 2018. 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 Human Design Medical, LLC in the registry?
The most recently registered devices listed for Human Design Medical, LLC include Z1 CPAP SYSTEM.