Saferay Spine, LLC
United StatesFDA applicant, unverified
- Devices
- 3
What Saferay Spine, LLC makes
Saferay Spine, LLC manufactures the LESSRAY system, including versions with and without tracking capabilities, designed for spinal procedures. These devices are intended for minimally invasive surgical applications in the spine.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Lessray Ref K123226
Regimes: 510(k) Registry: 510(k)LessRay with Tracking Ref K142243
Regimes: 510(k) Registry: 510(k)Lessray Ref K132970
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Saferay Spine, LLC have in the registry?
The registry currently lists 3 devices for Saferay Spine, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Saferay Spine, LLC's devices?
Among its 3 most recently registered devices, Saferay Spine, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Saferay Spine, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Saferay Spine, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Saferay Spine, LLC in the registry?
The most recently registered devices listed for Saferay Spine, LLC include LESSRAY and LessRay with Tracking.