FDA applicant

Starplex Scientific, Inc.

Etobicoke, Ontario, CA11 decisions1992–20030 recalls

FDA records 11 decisions for Starplex Scientific, Inc. (Etobicoke, Ontario, CA) from 1992 to 2003: 11 510(k) clearances. Most are in product codes JKA (Tubes, Vials, Systems, Serum Separators, Blood…) and JSM (Culture Media, Non-Propagating Transport). Its devices cite 5 predicates, 1 of them its own earlier devices. 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, clinical chemistry panel, where it files most

How often FDA has decided Starplex Scientific, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Starplex Scientific, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Starplex Scientific, Inc.’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) Report

Starplex Scientific, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?