Data / Medical devices / Israel / Dilon Medical Technologies Ltd.
Dilon Medical Technologies Ltd.: FDA-registered device maker in Caesarea Haifa, Israel, 1 PMA approval
Dilon Medical Technologies Ltd. is registered with the FDA (registration 3005755031) in Caesarea Haifa, Israel. It lists 1 device type. The FDA files 1 PMA approval under its listings, the newest dated December 27, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005755031
- Address
- 20 Alon Hatavor St., P.O.Box 3131, Caesarea Haifa, Israel, 3079519
- Owner or operator
- Dilon Medical Technologies, Inc (10042864)
- Roles
- Manufacturer
- First device listed
- January 8, 2013
- Registered through
- 2026
- Brand names listed
- MarginProbe Console, MarginProbe Probe, MarginProbe System
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Diagnostic Low Electric Field | OEE | 3 | Manufacturer | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| December 27, 2012 | P110014 | DUNE MEDICAL DEVICES MARGINPROBE SYSTEM | OEE | 13 | September 17, 2025 | accessdata.fda.gov |
Updated September 17, 2025. 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.