Data / Medical devices / Israel / El Global Trade Ltd.
El Global Trade Ltd.: FDA-registered device maker in Netanya Central, Israel, 11 510(k) clearances
El Global Trade Ltd. is registered with the FDA (registration 3011070163) in Netanya Central, Israel. It lists 6 device types. The FDA files 11 510(k) clearances under its listings, the newest dated May 23, 2025. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3011070163
- Address
- 13 Gibore Israel St., Netanya Central, Israel, 4250413
- Owner or operator
- EL Global Trade Ltd. (10047610)
- Roles
- Manufacturer, Specification developer
- First device listed
- October 12, 2014
- Registered through
- 2027
- Brand names listed
- CurrentBody Skin Radio Frequency Device, IPL400, SensiLight Mini, Sensica, Sensifirm, Sensifirm Pro, Sensilift, Sensilight Ice and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Light Based Over-The-Counter Hair Removal | OHT | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Massager, Therapeutic, Electric | ISA | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Massager, Vacuum, Radio Frequency Induced Heat | PBX | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction | PAY | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | ONF | 2 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| May 23, 2025 | K250384 | IPL400 | OHT | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| March 6, 2024 | K232424 | CurrentBody Skin RF | PAY | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| March 18, 2019 | K183260 | Sensilight Pro / Pistol IPL | OHT | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| September 19, 2018 | K181734 | Beurer IPL 8500 device/ IPL VelvetSkin Pro | OHT | Substantially Equivalent | Home Well Trading, Ltd. | accessdata.fda.gov |
| June 28, 2018 | K181121 | Beurer IPL 5500 device/ IPL 5000/ IPL PureSkin Pro | OHT | Substantially Equivalent | Home Well Trading, Ltd. | accessdata.fda.gov |
| October 13, 2017 | K172181 | micro IPL | OHT | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| July 14, 2017 | K170637 | sensiFirm | PBX | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| June 15, 2017 | K170499 | sensiLift | PAY | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| July 8, 2016 | K161089 | sensiLight Mini | OHT | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| August 8, 2014 | K140381 | SENSILIGHT/ SENSILIGHT PLUS | OHT | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
| July 31, 2014 | K140527 | SENSILIGHT MINI | OHT | Substantially Equivalent | El Global Trade, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Electrosurgical, Cutting & Coagulation & Accessories
- All makers of Massager, Vacuum, Radio Frequency Induced Heat
- All makers of Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction
- All makers of Light Based Over-The-Counter Hair Removal
- All makers of Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- All makers of Massager, Therapeutic, Electric
Updated May 23, 2025. 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.