FDA applicant

Pearl Instruments Corp.

Highland Park, IL2 decisions1989–19900 recalls

FDA records 2 decisions for Pearl Instruments Corp. (Highland Park, IL) from 1989 to 1990: 2 510(k) clearances. All are in product code GWM (Device, Monitoring, Intracranial Pressure). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Pearl Instruments Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pearl Instruments 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 “Pearl”

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

Pearl, Inc. 8 Pearl Diagnostics, Inc. 1 Pearl Digital, Inc. 1

Pearl Instruments Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pearl”