FDA applicant

Norland Corp.

Fort Atkinson, WI15 decisions1979–19980 recalls

FDA records 15 decisions for Norland Corp. (Fort Atkinson, WI) from 1979 to 1998: 15 510(k) clearances. All are in product code KGI (Densitometer, Bone). Its devices cite 7 predicates, 5 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 Norland Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Norland Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Norland”

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

Norland Medical Systems, Inc. 3

Norland Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Norland”