FDA applicant
The Daniels Corp.
FDA records 2 decisions for The Daniels Corp. (San Diego, CA) from 2000 to 2009: 2 510(k) clearances. All are in product code MMK (Container, Sharps). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Daniels Corporation Pty, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided The Daniels Corp.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2009
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like The Daniels Corp.’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 “The”
FDA records each applicant name separately; these may or may not be the same firm.