FDA applicant

Delaware Prosthetics, Inc.

Walker, MI5 decisions1983–19830 recalls

FDA records 5 decisions for Delaware Prosthetics, Inc. (Walker, MI) in 1983: 5 510(k) clearances. Most are in product codes GBI (Material, External Aesthetic Restoration, Used…) and FWP (Prosthesis, Chin, Internal). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Delaware Prosthetics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Delaware Prosthetics, 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 “Delaware”

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

Delaware Industries, Inc. 1

Delaware Prosthetics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Delaware”