Data / Medical devices / Israel / Body Vision Medical Lungvision Tool Manufacturing
Body Vision Medical Lungvision Tool Manufacturing: FDA-registered device maker in Netanya Northern, Israel, 1 510(k) clearance
Body Vision Medical Lungvision Tool Manufacturing is registered with the FDA (registration 3023214418) in Netanya Northern, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 26, 2018. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3023214418
- Address
- 4a H`azoran St., Netanya Northern, Israel, 4250604
- Owner or operator
- Body Vision Medical LungVision Tool Manufacturing (10085426)
- Roles
- Manufacturer
- First device listed
- June 16, 2022
- Registered through
- 2026
- Brand names listed
- LungVison Tool
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bronchoscope (Flexible Or Rigid) | EOQ | 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 |
|---|---|---|---|---|---|---|
| April 26, 2018 | K172955 | LungVision Tool | EOQ | Substantially Equivalent | Bodyvision Medical , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated April 26, 2018. 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.