Lifecare, Ltd.
IsraelFDA applicant, unverified
Lifecare, Ltd. is a medical device manufacturer, with 3 devices listed in FDA 510(k) (FDA Class II) as of 15 Nov 2026.
- Devices
- 3
Registry facts
- Registries
- FDA 510(k) 3
- Device classes
- FDA Class II 3
What Lifecare, Ltd. makes
Lifecare, Ltd. manufactures transcutaneous electrical nerve stimulation (TENS) systems, including reusable electrical connection cables and single-use or reusable electrodes for pain management. Their portfolio includes TENS devices, conductive gel pads, and specialized electrode designs like flower-patterned pads, alongside USB-enabled units for portable use.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) and UDI pathways.
Catalogue
Lifecare Compact Tens Device Ref K003369
Regimes: 510(k) Registry: 510(k)Livia Ref K163153
Regimes: 510(k) Registry: 510(k)Livia Ref K183110
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifecare, Ltd. have in the registry?
The registry currently lists 3 devices for Lifecare, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifecare, Ltd.'s devices?
Among its 3 most recently registered devices, Lifecare, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Lifecare, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lifecare, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifecare, Ltd. in the registry?
The most recently registered devices listed for Lifecare, Ltd. include LIFECARE COMPACT TENS DEVICE and Livia.