FDA applicant

Northeast Iowa Podiatry

Waterloo, IA1 decision1985–19850 recalls

FDA records 1 decision for Northeast Iowa Podiatry (Waterloo, IA) in 1985: 1 510(k) clearance. All are in product code HWC (Screw, Fixation, Bone). 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, orthopedic panel, where it files most

How often FDA has decided Northeast Iowa Podiatry’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Northeast Iowa Podiatry since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Northeast”

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

Northeast Biomedical Labs., Inc. 9 Northeast Scientific, Inc. 6 Northeast Scientific, Inc. (Nes) 1 Northeast Orthotics and Prothetics, Inc. 1 Northeast Resins & Silicones, LLC 1

Northeast Iowa Podiatry

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Northeast”