Data / Medical devices / Israel / Synchrony Medical Ltd
Synchrony Medical Ltd: FDA-registered device maker in Or Yehuda Tel Aviv, Israel, 1 510(k) clearance
Synchrony Medical Ltd is registered with the FDA (registration 3035523355) in Or Yehuda Tel Aviv, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 19, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3035523355
- Address
- 8 Ariel Sharon st., Or Yehuda Tel Aviv, Israel, 6037606
- Owner or operator
- Synchrony Medical Ltd (10092400)
- Roles
- Manufacturer
- First device listed
- January 2, 2025
- Registered through
- 2026
- Brand names listed
- LibAirty Airway Clearance System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Percussor, Powered-Electric | BYI | 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 |
|---|---|---|---|---|---|---|
| December 19, 2024 | K242063 | LibAirty Airway Clearance System | BYI | Substantially Equivalent | Synchrony Medical , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated December 19, 2024. 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.