Data / Medical devices / United States / Dilon Technologies Inc
Dilon Technologies Inc: FDA-registered device maker in Newport News, VA, United States, 1 PMA approval
Dilon Technologies Inc is registered with the FDA (registration 1125612) in Newport News, VA, United States. It lists 3 device types. The FDA files 1 PMA approval under its listings, the newest dated December 15, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1125612
- FEI number
- 3002931663
- Address
- 701 Mariners Row, Suite 200, Newport News, VA, United States, 23606
- Owner or operator
- DILON TECHNOLOGIES Inc (9035906)
- Roles
- Complaint file establishment, Manufacturer, Specification developer
- First device listed
- April 14, 2014
- Registered through
- 2026
- Brand names listed
- CoPilot VL, GPS Navigator with Probes, HEMOBLAST Bellows, NAVIGATOR 2 with Wired and Wireless Probe
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Absorbable Collagen Hemostatic Agent With Thrombin | PMX | 3 | Complaint file establishment | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Probe, Uptake, Nuclear | IZD | 1 | 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 15, 2017 | P170012 | HEMOBLAST Bellows | PMX | 32 | September 3, 2026 | accessdata.fda.gov |
Compare with other makers
- All makers of Laryngoscope, Rigid
- All makers of Probe, Uptake, Nuclear
- All makers of Absorbable Collagen Hemostatic Agent With Thrombin
Updated September 3, 2026. 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.