Osspray, Ltd.
Country not established
- Devices
- 2
What Osspray, Ltd. makes
Osspray, Ltd. manufactures the OSSPRAY SYLC CR, a Class I surgical device designed for bone preparation in orthopedic procedures, and the SYLE SMARTIP, a Class I intramedullary rod for fracture fixation in long bones.
These devices are regulated under the FDA’s 510(k) pathway as Class I medical devices and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Osspray Sylc Cr Ref K103114
Regimes: 510(k) Registry: 510(k)Syle Smartip Ref K100833
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osspray, Ltd. have in the registry?
The registry currently lists 2 devices for Osspray, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osspray, Ltd.'s devices?
Among its 2 most recently registered devices, Osspray, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Osspray, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Osspray, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Osspray, Ltd. in the registry?
The most recently registered devices listed for Osspray, Ltd. include OSSPRAY SYLC CR and SYLE SMARTIP.