FDA applicant

Exakt Medical Instruments, Inc.

Oklahoma City, OK1 decision1988–19880 recalls

FDA records 1 decision for Exakt Medical Instruments, Inc. (Oklahoma City, OK) in 1988: 1 510(k) clearance. All are in product code IDP (Microtome, Cryostat). 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, pathology panel, where it files most

How often FDA has decided Exakt Medical Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Exakt Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Exakt Medical Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?