FDA applicant

Safeway Products, Inc.

Middletown, CT3 decisions1982–19890 recalls

FDA records 3 decisions for Safeway Products, Inc. (Middletown, CT) from 1982 to 1989: 3 510(k) clearances. Most are in product codes HPX (Lens, Contact (Polymethylmethacrylate)) and LYY (Latex Patient Examination Glove). 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, general hospital panel, where it files most

How often FDA has decided Safeway Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Safeway Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Safeway Products, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Safeway”

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

Safeway Industry Healthcare. 1

Safeway Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Safeway”