510(k) Report

FDA applicant

The Daniels Corp.

San Diego, CA2 decisions2000–20090 recalls

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, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided The Daniels Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Daniels Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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Other applicant names beginning “The”

FDA records each applicant name separately; these may or may not be the same firm.