FDA applicant

Sutter Corp.

San Diego, CA7 decisions1989–19950 recalls

FDA records 7 decisions for Sutter Corp. (San Diego, CA) from 1989 to 1995: 7 510(k) clearances. Most are in product codes BXB (Exerciser, Powered) and KWH (Prosthesis, Toe, Constrained, Polymer). 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 Sutter Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sutter Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sutter Corp.’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 “Sutter”

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

Sutter Biomedical, Inc. 11 Sutter Medizintechnik GmbH 9

Sutter Corp.

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 “Sutter”