Data / Medical devices / Israel / Talshir Guy Medical Technologies Ltd.
Talshir Guy Medical Technologies Ltd.: FDA-registered device maker in Modiin Central, Israel, 1 510(k) clearance
Talshir Guy Medical Technologies Ltd. is registered with the FDA (registration 3012185572) in Modiin Central, Israel. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 31, 2001. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3012185572
- Address
- 4 Izdarechet St, Modiin Central, Israel, 7176112
- Owner or operator
- Talshir Guy Medical Technologies Ltd. (10050633)
- Roles
- Manufacturer
- First device listed
- December 10, 2015
- Registered through
- 2026
- Brand names listed
- RevitalVision
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Haploscope | HJT | 1 | 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 |
|---|---|---|---|---|---|---|
| August 31, 2001 | K012530 | AA-1 SYSTEM | HJT | Substantially Equivalent | Neurovision, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 31, 2001. 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.