FDA applicant

Shepherd Laboratories, Inc.

Djolla, CA1 decision1997–19970 recalls

FDA records 1 decision for Shepherd Laboratories, Inc. (Djolla, CA) in 1997: 1 510(k) clearance. All are in product code FPA (Set, Administration, Intravascular). 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 Shepherd Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shepherd Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Shepherd Laboratories, 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 “Shepherd”

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

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

Shepherd Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Shepherd”