Xplr, Ltd.
IsraelFDA 510(k) applicant, unverified
- Devices
- 2
What Xplr, Ltd. makes
Xplr, Ltd. manufactures the LMNT O2, a medical device designed for oxygen monitoring and delivery in clinical or portable settings.
The LMNT O2 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- GUDID
Lmnt O2 Ref K250125
510(k) 510(k)
Company details
- DUNS number
- 626512683
Frequently asked questions
How many devices does Xplr, Ltd. have in the registry?
The registry currently lists 2 devices for Xplr, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xplr, Ltd.'s devices?
Among its 2 most recently registered devices, Xplr, Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Xplr, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Xplr, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xplr, Ltd. in the registry?
The most recently registered devices listed for Xplr, Ltd. include LMNT O2.