FDA applicant

Clover Hi-Tech, Inc.

City Of Industry, CA1 decision2003–20030 recalls

FDA records 1 decision for Clover Hi-Tech, Inc. (City Of Industry, CA) in 2003: 1 510(k) clearance. All are in product code DQK (Computer, Diagnostic, Programmable). 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, cardiovascular panel, where it files most

How often FDA has decided Clover Hi-Tech, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Clover Hi-Tech, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Clover Hi-Tech, 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 “Clover”

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

Clover Medical Equipment Services, Inc. 1 Clover Glove Company Limited 1

Clover Hi-Tech, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Clover”