Data / Medical devices / Israel / Admetec Solution Ltd
Admetec Solution Ltd: FDA-registered device maker in Haifa, Israel, 1 510(k) clearance
Admetec Solution Ltd is registered with the FDA (registration 3014414462) in Haifa, Israel. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 12, 1989. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014414462
- Address
- Yokhanan HaSandlar St. 18, Haifa, Israel, 3296218
- Owner or operator
- Admetec Solution LTD (10081840)
- Roles
- Manufacturer
- First device listed
- May 20, 2021
- Registered through
- 2026
- Brand names listed
- Admetec Loupes, Butterfly, Flamingo w/camera, Orchid
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Light, Examination, Medical, Battery Powered | KYT | 1 | Manufacturer | accessdata.fda.gov |
| Loupe, Diagnostic/Surgical | FSP | 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 |
|---|---|---|---|---|---|---|
| April 12, 1989 | K891895 | SURGICAL LOUPES | FSP | Substantially Equivalent | Zinnanti Surgical Instruments, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 12, 1989. 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.