FDA applicant
Athena Technology, Inc.
FDA records 3 decisions for Athena Technology, Inc. (San Dimas, CA) from 1994 to 1998: 3 510(k) clearances. All are in product code EFB (Handpiece, Air-Powered, Dental). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Athena Technology, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Athena Technology, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Athena Technology, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Athena”
FDA records each applicant name separately; these may or may not be the same firm.