FDA applicant

Sierra Medical Devices

Grass Valley, CA2 decisions1992–19960 recalls

FDA records 2 decisions for Sierra Medical Devices (Grass Valley, CA) from 1992 to 1996: 2 510(k) clearances. 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 Sierra Medical Devices’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sierra Medical Devices since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Sierra”

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

Sierra Laboratories, Inc. 12 Sierra Scientific Instruments, Inc. 2 Sierra Corp. 1 Sierra Diagnostic, LLC 1 Sierra Biosearch, Inc. 1 Sierra Diagnostics 1 Sierra Surgical, Inc. 1 Sierra Battery, Inc. 1

Sierra Medical Devices

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sierra”