FDA applicant

Sakura Finetek U.S.A., Inc.

Torrance, CA4 decisions1988–19890 recalls

FDA records 4 decisions for Sakura Finetek U.S.A., Inc. (Torrance, CA) from 1988 to 1989: 4 510(k) clearances. Most are in product codes KPA (Slide Stainer, Automated) and KES (Coverslips, Microscope Slide). 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, pathology panel, where it files most

How often FDA has decided Sakura Finetek U.S.A., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Sakura Finetek U.S.A., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Sakura Finetek U.S.A., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Sakura Finetek U.S.A., 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 “Sakura”

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

Sakura Seiki Co., Ltd. 3

Sakura Finetek U.S.A., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Sakura”