Data / Medical devices / Israel / Nanovibronix, Ltd.
Nanovibronix, Ltd.: FDA-registered device maker in NESHER Haifa, Israel, 1 510(k) clearance
Nanovibronix, Ltd. is registered with the FDA (registration 3006262007) in NESHER Haifa, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 22, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006262007
- Address
- 47, Ha-Ta'Asiya, NESHER Haifa, Israel, 3688847
- Owner or operator
- NANOVIBRONIX, LTD. (9102520)
- Roles
- Specification developer
- First device listed
- September 16, 2008
- Registered through
- 2026
- Brand names listed
- PainShield MD
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stationary Ultrasonic Diathermy Device For Use In Applying Therapeutic Deep Heat | PFW | 2 | Specification developer | 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 22, 2008 | K081075 | PAINSHIELD MD | PFW | Substantially Equivalent | Nano Vibronix , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 22, 2008. 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.