FDA applicant

Elite Technology, Inc.

Canada M9w 5p1, CA5 decisions1990–19900 recalls

FDA records 5 decisions for Elite Technology, Inc. (Canada M9w 5p1, CA) in 1990: 5 510(k) clearances. Most are in product codes KNK (Acid, Uric, Uricase (Colorimetric)) and JPZ (Colorimetric Method, Gamma-Glutamyl…). 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 Elite Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Elite Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Elite”

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

Elite Diagnostic, Ltd. 5 Elite Surgical Supplies (Pty), Ltd. 4 Elite International, Inc. 4 Elite Electromedical 1 Elite Biomedical Solutions 1 Elite Medical Supply of New York, LLC 1 Elite Medical, Inc. 1

Elite Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Elite”