Data / Medical devices / Massager, Therapeutic, Electric / Israel
FDA-registered makers of Massager, Therapeutic, Electric in Israel: 11 establishments
11 establishments in Israel are registered with the FDA to make Massager, Therapeutic, Electric (product code ISA). 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
- Massager, Therapeutic, Electric
- Product code
- ISA
- Country
- Israel
Makers of Massager, Therapeutic, Electric in Israel
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alma Lasers Ltd. | CAESAREA Northern, Israel | Complaint file establishment, Manufacturer | 1 | January 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Medispec, Ltd. | YEHUD Central, Israel | Manufacturer | 1 | January 27, 2023 | 0 | 0 | 0 | api.fda.gov |
| Aerotel Ltd. | Holon Central, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| B.Y. Medimor Ltd | Tiberias Northern, Israel | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Curatronic, Ltd. | JERUSALEM Central, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| El Global Trade Ltd. | Netanya Central, Israel | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Initia, Ltd. | Petah Tikva Central, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inmode Ltd. | Yokneam Northern, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pollogen Ltd | Tel Aviv, Israel | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| R.H. Electronics Ltd. | Nof Hagalil Northern, Israel | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Viora Ltd. | Migdal HaEmek Northern, Israel | Complaint file establishment, Exporter to the US, 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.