St. George Technology, Inc.
Wilmington, NC, US
ST. GEORGE TECHNOLOGY, INC. appears in FDA device records in Wilmington, NC. FDA records list 4 510(k) clearances between and , no 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 4 510(k) clearances for St. George Technology, Inc. between 1994 and 2003. The busiest year on record is 1994, with 1. The most recent is 2003, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 1 |
| 1995 | 1 |
| 2000 | 1 |
| 2003 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K023953 | ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE | EGS | Substantially Equivalent | |
| K992176 | EXCEL ULTRA-HI FORMULA HEAT-CURED DENTURE BASE MATERIAL | EBI | Substantially Equivalent | |
| K945711 | EXCEL-P FORMULA AUTO-CURE DENTURE BASE | EBI | Substantially Equivalent | |
| K934019 | EXCEL FORMULA HEAT-AUTO CURE DENT BASE/REPAIR/ORTHO | EBI | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2530024 | 1000161170 | ST. GEORGE TECHNOLOGY, INC. | 210 N. GREEN MEADOWS DRIVE, Wilmington, NC 28405 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