510(k) Report

FDA applicant

Apollo Dental Products, Inc.

Fresno, CA2 decisions1985–19880 recalls

FDA records 2 decisions for Apollo Dental Products, Inc. (Fresno, CA) from 1985 to 1988: 2 510(k) clearances. All are in product code EIA (Unit, Operative Dental). 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 Apollo Dental Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Apollo Dental Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Apollo Dental 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 “Apollo”

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