FDA applicant

Special Devices, Inc.

Grass Valley, CA2 decisions1998–20050 recalls

FDA records 2 decisions for Special Devices, Inc. (Grass Valley, CA) from 1998 to 2005: 2 510(k) clearances. Most are in product codes MDM (Instrument, Manual, Surgical, General Use) and HTN (Washer, Bolt Nut). 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 Special Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Special Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Special Devices, 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 “Special”

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

Special Health Systems, Ltd. 3 Special Machinery Co. 1 Special Products, Inc. 1 Special Medical Co., Ltd. 1 Special Situations, LLC 1

Special Devices, 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 “Special”