Data / Medical devices / Israel / Nonagon Ltd.
Nonagon Ltd.: FDA-registered device maker in Caesarea Haifa, Israel, 1 510(k) clearance
Nonagon Ltd. is registered with the FDA (registration 3018783553) in Caesarea Haifa, Israel. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 23, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3018783553
- Address
- 1 HaEshel Street, Caesarea Haifa, Israel, 3079830
- Owner or operator
- Nonagon Ltd. (10081507)
- Roles
- Manufacturer
- First device listed
- April 21, 2021
- Registered through
- 2026
- Brand names listed
- Nonagon N9+ Accessories Kit, Nonagon N9+ Kit
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Otoscope | ERA | 1 | Manufacturer | accessdata.fda.gov |
| Oximeter | DQA | 2 | Manufacturer | accessdata.fda.gov |
| Specula Accessories | FXG | 1 | Manufacturer | accessdata.fda.gov |
| Stethoscope, Electronic | DQD | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 23, 2021 | K202483 | MyHomeDoc | DQD | Substantially Equivalent | Myhomedoc , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Otoscope
- All makers of Oximeter
- All makers of Continuous Measurement Thermometer
- All makers of Stethoscope, Electronic
- All makers of Specula Accessories
Updated March 23, 2021. 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.