MedMinder Systems, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3007729562
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 1
Catalogue
- Registry: GUDID
Company details
- FDA FEI number
- 3007729562
- Address
- 320 Norwood Park S., Norwood, MA, 02062
FDA recalls
Recalls initiated per year
- 2017 0
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 1
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2022
- 28 Mar 2022 Z-1254-2022 Class II Terminated Discontinuation of the Emergency Alert watch or pendant will no longer connect to the emergency alert system for all models. Older Model (legacy) without screen medical alert feature(button) removed
Frequently asked questions
How many devices does MedMinder Systems, Inc. have in the registry?
The registry currently lists 1 device for MedMinder Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list MedMinder Systems, Inc.'s devices?
Among its 1 most recently registered device, MedMinder Systems, Inc. has devices listed in FDA GUDID (1 device).
What risk classes do MedMinder Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for MedMinder Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for MedMinder Systems, Inc.?
FDA recall records list 1 recall initiated by MedMinder Systems, Inc., the most recent initiated on 28 Mar 2022. 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 MedMinder Systems, Inc. in the registry?
The most recently registered devices listed for MedMinder Systems, Inc. include MedMinder Systems, Inc. ORI 3.