FDA applicant

Sierra Battery, Inc.

Reno, NV1 decision1995–19950 recalls

FDA records 1 decision for Sierra Battery, Inc. (Reno, NV) in 1995: 1 510(k) clearance. All are in product code IZL (System, X-Ray, Mobile). 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, radiology panel, where it files most

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

FDA decisions per year

No FDA decision for Sierra Battery, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sierra Battery, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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 Medical Devices 2 Sierra Corp. 1 Sierra Diagnostic, LLC 1 Sierra Biosearch, Inc. 1 Sierra Diagnostics 1 Sierra Surgical, Inc. 1

Sierra Battery, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sierra”