Sls Biophile, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Sls Biophile, Ltd. makes
Sls Biophile, Ltd. manufactures the NLITE System (SLS model number A00-1025), a medical device designed for specific clinical applications requiring controlled light exposure.
The NLITE System is classified as a Class II device under FDA regulations and is listed in the 510(k) registry. The company is based in the United States.
Catalogue
Nlite System, Sls Model Number A00-1025 Ref K000811
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sls Biophile, Ltd. have in the registry?
The registry currently lists 1 device for Sls Biophile, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sls Biophile, Ltd.'s devices?
Among its 1 most recently registered device, Sls Biophile, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Sls Biophile, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sls Biophile, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sls Biophile, Ltd. in the registry?
The most recently registered devices listed for Sls Biophile, Ltd. include NLITE SYSTEM, SLS MODEL NUMBER A00-1025.