510(k) Report

FDA applicant

Imation Corp.

Oakdale, MN5 decisions1996–19990 recalls

FDA records 5 decisions for Imation Corp. (Oakdale, MN) from 1996 to 1999: 5 510(k) clearances. Most are in product codes LMD (System, Digital Image Communications…) and IXA (Cassette, Radiographic Film). Its devices cite 3 predicates, 0 of them its own earlier devices. 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Imation Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Imation 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 “Imation”

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