Data / Medical devices / United States / DILON MEDICAL TECHNOLOGIES, Inc
DILON MEDICAL TECHNOLOGIES, Inc: FDA-registered device maker in Newport News, VA, United States, 1 PMA approval
DILON MEDICAL TECHNOLOGIES, Inc is registered with the FDA (registration 3010060126) in Newport News, VA, United States. 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
- 3010060126
- Address
- 701 Mariners Row Suite 200, Newport News, VA, United States, 23606
- Owner or operator
- Dilon Medical Technologies, Inc (10042981)
- Roles
- Complaint file establishment
- First device listed
- January 17, 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 | Complaint file establishment | 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.