510(k) Report

FDA applicant

Signature One Products, Inc.

Boca Raton, FL1 decision1990–19900 recalls

FDA records 1 decision for Signature One Products, Inc. (Boca Raton, FL) in 1990: 1 510(k) clearance. All are in product code DZA (Drill, Dental, Intraoral). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Signature One Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Signature One Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Signature One Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Signature One Products, Inc.’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 “Signature”

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