FDA applicant

Norman R. Sanborn Co.

Mchenry, IL1 decision1979–19790 recalls

FDA records 1 decision for Norman R. Sanborn Co. (Mchenry, IL) in 1979: 1 510(k) clearance. All are in product code FQM (Bandage, Elastic). 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 Norman R. Sanborn Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Norman R. Sanborn Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Norman R. Sanborn Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Norman R. Sanborn Co.’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 “Norman”

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

Norman'S 1 Norman M. Black Iii 1

Norman R. Sanborn Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Norman”