FDA applicant

Keller Instruments, Inc.

Mchenry, IL5 decisions1983–19850 recalls

FDA records 5 decisions for Keller Instruments, Inc. (Mchenry, IL) from 1983 to 1985: 5 510(k) clearances. Most are in product codes HQA (Unit, Cryotherapy, Ophthalmic) and HLT (Preamplifier, Ac-Powered, 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 Keller Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Keller Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Keller Instruments, 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 “Keller”

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

Keller Medical Specialties Products, Inc. 6

Keller Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Keller”