Vickers America Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 22
What Vickers America Medical Corp. makes
The company manufactures neonatal and pediatric medical devices, including ventilators (e.g., SP 120 Sophisticate, Treonic C30), incubators (e.g., NeoCare Baby-Controlled Incubator), and respiratory support systems like PEEP/CPAP valves. Additional products include neonatal apnea monitoring systems (e.g., VMA Pediatric Apnea Mattress), temperature and oxygen monitors (e.g., NeoCare Temperature Monitor, NeoCare Oxygen Monitor), and resuscitation devices (e.g., Resuscitaire). Laboratory data management systems (e.g., SDMS) and specialized neonatal ventilators (e.g., Vickers Medical Model 130 Neavent-Neo) are also part of the portfolio.
The portfolio includes devices regulated as Class I and Class II under FDA 510(k) requirements. Products are listed in the FDA’s 510(k) clearance registry, reflecting their compliance with U.S. medical device regulations. The company is based in the United States.
Catalogue
Search and filter all 22 devicesFrequently asked questions
How many devices does Vickers America Medical Corp. have in the registry?
The registry currently lists 22 devices for Vickers America Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vickers America Medical Corp.'s devices?
Among its 22 most recently registered devices, Vickers America Medical Corp. has devices listed in FDA 510(k) (22 devices).
What risk classes do Vickers America Medical Corp.'s devices fall under?
Among its 22 most recently registered devices, the classes recorded for Vickers America Medical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vickers America Medical Corp. in the registry?
The most recently registered devices listed for Vickers America Medical Corp. include SP 120 SOPHISTICATE, NEOCARE BABY-CONTROLLED INCUBATOR, TREONIC IP5 and PEEP/CPAP VALVE.