FDA applicant

Corning Costar Corp.

Mchenry, IL8 decisions1980–19870 recalls

FDA records 8 decisions for Corning Costar Corp. (Mchenry, IL) from 1980 to 1987: 8 510(k) clearances. Most are in product codes JTC (Device, Microtiter Diluting/Dispensing) and KJA (Flask, Tissue Culture). 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, microbiology panel, where it files most

How often FDA has decided Corning Costar Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Corning Costar Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Corning”

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

Corning Medical & Scientific 111 Corning Nichols Diagnostics 1

Corning Costar Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Corning”