Data / Medical devices / Device, Biofeedback / Israel
FDA-registered makers of Device, Biofeedback in Israel: 5 establishments
5 establishments in Israel are registered with the FDA to make Device, Biofeedback (product code HCC). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Device, Biofeedback
- Product code
- HCC
- Country
- Israel
Makers of Device, Biofeedback in Israel
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 2breathe Technologies Ltd | Raanana Central, Israel | Specification developer | 1 | July 2, 2002 | 0 | 0 | 0 | api.fda.gov |
| Graymatters Health | Haifa, Israel | Manufacturer | 1 | March 17, 2023 | 0 | 0 | 0 | api.fda.gov |
| Appscent Medical | Raanana Central, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| I-Braintech Ltd | Tel Aviv-Yafo, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tavger Ltd. | Katzrin Ha Zafon Haifa, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.