Data / Medical devices / Israel / Nurami Medical Ltd
Nurami Medical Ltd: FDA-registered device maker in Haifa, Israel, 1 510(k) clearance
Nurami Medical Ltd is registered with the FDA (registration 3030126381) in Haifa, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 10, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030126381
- Address
- 36, Ha-Namal, Haifa, Israel, 3303203
- Owner or operator
- Nurami Medical Ltd (10089552)
- Roles
- Manufacturer
- First device listed
- December 17, 2023
- Registered through
- 2026
- Brand names listed
- ArtiFascia 3X4, ArtiFascia 5X5, ArtiFascia 7X7
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dura Substitute | GXQ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 10, 2023 | K223445 | ArtiFascia | GXQ | Substantially Equivalent | Nurami Medical , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 10, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.