FDA applicant

Strieter Clinical Research Laboratories, Inc.

Collinsville, IL1 decision2000–20000 recalls

FDA records 1 decision for Strieter Clinical Research Laboratories, Inc. (Collinsville, IL) in 2000: 1 510(k) clearance. All are in product code LYL (Accessories, Solution, Ultrasonic Cleaners For…). 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, ophthalmic panel, where it files most

How often FDA has decided Strieter Clinical Research Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Strieter Clinical Research Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Strieter Clinical Research Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?