Data / Medical devices / Israel / BeamMed Ltd.
BeamMed Ltd.: FDA-registered device maker in Petah Tikva Central, Israel, 1 510(k) clearance
BeamMed Ltd. is registered with the FDA (registration 3006701790) in Petah Tikva Central, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 12, 2011. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3006701790
- Address
- 8 Ha-Lapid Street, Petah Tikva Central, Israel, 4925822
- Owner or operator
- BeamMed Ltd (10024010)
- Roles
- Manufacturer
- First device listed
- November 23, 2011
- Registered through
- 2027
- Brand names listed
- Sunlight MiniOmni
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bone Sonometer | MUA | 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 |
|---|---|---|---|---|---|---|
| October 12, 2011 | K110646 | BEAMMED SUNLIGHT MINIOMNI BONE SONOMETER | MUA | Substantially Equivalent | Beam-Med, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 12, 2011. 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.