Vitalgo Inc.
Country not established FDA establishment FEI 3010034871
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 1
Catalogue
- GUDID
Company details
- FDA FEI number
- 3010034871
- Address
- 3315 Commerce Pkwy, Miramar, FL, 33025
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
- 12 Apr 2018 Z-2739-2018 Class II Terminated Potential for unintentional movement of the support surface of the bed from tilted position to horizontal position or any position in between.
Frequently asked questions
How many devices does VITALGO INC. have in the registry?
The registry currently lists 1 device for VITALGO INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VITALGO INC.'s devices?
Among its 1 most recently registered device, VITALGO INC. has devices listed in FDA GUDID (1 device).
What risk classes do VITALGO INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for VITALGO INC.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for VITALGO INC.?
FDA recall records list 1 recall initiated by VITALGO INC., the most recent initiated on 2018-04-12. 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 VITALGO INC. in the registry?
The most recently registered devices listed for VITALGO INC. include TLB TLB425T.