Elastimed Ltd
IsraelFDA 510(k) applicant, unverified FDA
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Elastimed Ltd makes
Elastimed, Ltd. manufactures sacral pressure-relief devices, including the SACS PRO and ElastiMed SACS, designed to reduce pressure injuries for patients requiring prolonged seating or bed rest.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Search and filter all 11 devicesCompany details
- DUNS number
- 600461703
- [email protected]
- Phone
- +1(844) 679-9100
FDA establishments
- Elastimed Yokneam Ilit Northern · IL FEI 3023215120
Frequently asked questions
How many devices does ELASTIMED LTD have in the registry?
The registry currently lists 11 devices for ELASTIMED LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list ELASTIMED LTD's devices?
Among its 11 most recently registered devices, ELASTIMED LTD has devices listed in FDA 510(k) (2 devices) and FDA GUDID (9 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ELASTIMED LTD's devices fall under?
Among its 11 most recently registered devices, the classes recorded for ELASTIMED LTD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ELASTIMED LTD in the registry?
The most recently registered devices listed for ELASTIMED LTD include MyoSleeve 1.0, SACS PRO 1.0, SACS PRO and ElastiMed SACS.
Which FDA establishments are linked to ELASTIMED LTD?
1 FDA establishment is linked to ELASTIMED LTD in the registry; they are listed on the company page.