FDA applicant

Connecticut Bioinstruments, Inc.

Danbury, CT1 decision1992–19920 recalls

FDA records 1 decision for Connecticut Bioinstruments, Inc. (Danbury, CT) in 1992: 1 510(k) clearance. All are in product code HJC (Esthesiometer, Ocular). 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 Connecticut Bioinstruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Connecticut Bioinstruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Connecticut Bioinstruments, 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 “Connecticut”

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

Connecticut Diagnostics, Ltd. 14

Connecticut Bioinstruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Connecticut”