Data / Medical devices / Powered Light Based Non-Laser Surgical Instrument With Thermal Effect / Israel
FDA-registered makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect in Israel: 10 establishments
10 establishments in Israel are registered with the FDA to make Powered Light Based Non-Laser Surgical Instrument With Thermal Effect (product code ONF). 4 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
- Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- Product code
- ONF
- Country
- Israel
Makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect in Israel
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alma Lasers Ltd. | CAESAREA Northern, Israel | Manufacturer | 2 | June 13, 2018 | 0 | 0 | 0 | api.fda.gov |
| Formatk Systems Ltd. | Tirat Hacarmel Northern, Israel | Manufacturer | 1 | April 15, 2016 | 0 | 0 | 0 | api.fda.gov |
| Inmode Ltd. | Yokneam Northern, Israel | Manufacturer | 1 | April 2, 2013 | 0 | 0 | 0 | api.fda.gov |
| Viora Ltd. | Migdal HaEmek Northern, Israel | Manufacturer | 1 | June 10, 2009 | 0 | 0 | 0 | api.fda.gov |
| Atena (from The Imco Group) Ltd | Nesher Haifa, Israel | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| B.Y. Medimor Ltd | Tiberias Northern, Israel | Contract 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 | |
| Lumenis Be Ltd | Yokneam, Ha Zafon 2069236 Haifa, Israel | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| R.H. Electronics Ltd. | Nof Hagalil Northern, Israel | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sharplight Technologies Ltd. | RISHON LEZION Tel Aviv, 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.