FDA applicant

Shepherd Medical Products, Inc.

Washington, DC1 decision1991–19910 recalls

FDA records 1 decision for Shepherd Medical Products, Inc. (Washington, DC) in 1991: 1 510(k) clearance. All are in product code IRP (Massager, Powered Inflatable Tube). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Shepherd Medical Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Shepherd”

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

Shepherd Scientific, Inc. 1 Shepherd Laboratories, Inc. 1 Shepherd Medical Corp. 1

Shepherd Medical Products, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Shepherd”