FDA applicant

Truline Instruments, Inc.

Mchenry, IL1 decision1984–19840 recalls

FDA records 1 decision for Truline Instruments, Inc. (Mchenry, IL) in 1984: 1 510(k) clearance. All are in product code HOB (Clamp, Muscle, 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 Truline Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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Truline Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?