Pedialift LLC
Country not established
- Devices
- 1
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Pedialift LLC makes
PediaLift LLC manufactures basic electric hospital beds designed for clinical use, including the PediaLift model tailored for pediatric and adult patients in healthcare settings. These beds provide adjustable positioning and mobility features to support patient care and comfort in hospital environments.
The company’s products fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States, adhering to applicable U.S. medical device compliance requirements.
Catalogue
- GUDID
Company details
- DUNS number
- 080045535
- [email protected]
- Phone
- 4195288180
FDA recalls
FDA recall records list 1 recall initiated by PEDIALIFT LLC, initiated on 2019-07-03. By recorded status: 1 terminated. The reasons filed fall into these groups: labeling or instructions for use. 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 1
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2019
- 3 Jul 2019 Z-0931-2020 Class II Terminated The firm was unsuccessful in obtaining a satisfactory Certificate of Conformance from the original vendor of the mattress showing that they are in compliance with labeling requirements.
Frequently asked questions
How many devices does PEDIALIFT LLC have in the registry?
The registry currently lists 1 device for PEDIALIFT LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list PEDIALIFT LLC's devices?
Among its 1 most recently registered device, PEDIALIFT LLC has devices listed in FDA GUDID (1 device).
What risk classes do PEDIALIFT LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for PEDIALIFT LLC's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for PEDIALIFT LLC?
FDA recall records list 1 recall initiated by PEDIALIFT LLC, the most recent initiated on 2019-07-03. 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 PEDIALIFT LLC in the registry?
The most recently registered devices listed for PEDIALIFT LLC include PediaLift.