Dilon Technologies Inc
Newport News, VA, US
DILON TECHNOLOGIES INC appears in FDA device records in Newport News, VA. FDA records list 3 510(k) clearances between and , 32 PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Dilon Technologies Inc between 1999 and 2011. The busiest year on record is 1999, with 1. The most recent is 2011, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1999 | 1 |
| 2009 | 1 |
| 2011 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K110384 | DILON 6800 ACELLA (ACELLA) | IYX | Substantially Equivalent | |
| K082588 | GAMMALOC SYSTEM, MODEL 03-00001 | IYX | Substantially Equivalent | |
| K984466 | DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5 | IYX | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 1125612 | 3002931663 | DILON TECHNOLOGIES INC | 701 Mariners Row, Suite 200, NEWPORT NEWS, VA 23606 US | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain