FDA applicant

Stephens Instruments

Lexington, KY5 decisions2002–20020 recalls

FDA records 5 decisions for Stephens Instruments (Lexington, KY) in 2002: 5 510(k) clearances. Most are in product codes HNF (Scissors, Ophthalmic) and HNQ (Hook, Ophthalmic). 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 Stephens Instruments’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Stephens Instruments since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Stephens”

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

Stephens Scientific 4 Stephens Mfg. Co. 1

Stephens Instruments

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Stephens”