FDA applicant

Polaroid Corp.

Mchenry, IL5 decisions1979–19810 recalls

FDA records 5 decisions for Polaroid Corp. (Mchenry, IL) from 1979 to 1981: 5 510(k) clearances. Most are in product codes FEM (Accessories, Photographic, For Endoscope…) and IXW (Processor, Radiographic-Film, Automatic). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Polaroid Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Polaroid 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 “Polaroid”

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

Polaroid Medical Corp. 1

Polaroid Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Polaroid”