510(k) Report

FDA applicant

Condor Products, Inc.

Yorba Linda, CA1 decision1996–19960 recalls

FDA records 1 decision for Condor Products, Inc. (Yorba Linda, CA) in 1996: 1 510(k) clearance. All are in product code ELC (Scaler, Ultrasonic). 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 Condor Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Condor Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Condor 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 “Condor”

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