Lerman & Son
Country not established
- Devices
- 1
What Lerman & Son makes
Lerman & Son manufactures cranial orthosis helmets designed for pediatric patients requiring external head protection and support, typically for conditions such as craniosynostosis or traumatic brain injury.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The manufacturer operates from the United States.
Catalogue
Lerman & Son Cranial Orthosis Helmet Ref K012830
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lerman & Son have in the registry?
The registry currently lists 1 device for Lerman & Son. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lerman & Son's devices?
Among its 1 most recently registered device, Lerman & Son has devices listed in FDA 510(k) (1 device).
What risk classes do Lerman & Son's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lerman & Son's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lerman & Son in the registry?
The most recently registered devices listed for Lerman & Son include LERMAN & SON CRANIAL ORTHOSIS HELMET.