FDA applicant

Sa Scientific, Inc.

San Antonio, TX201 decisions1993–20130 recalls

FDA records 201 decisions for Sa Scientific, Inc. (San Antonio, TX) from 1993 to 2013: 201 510(k) clearances. Most are in product codes GRM (Antisera, All Groups, Salmonella Spp.) and GNC (Antigens, Febrile, Slide And Tube, All Groups…). Its devices cite 6 predicates, 4 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Sa Scientific , Ltd.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, microbiology panel, where it files most

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

FDA decisions per year

1in 2013

2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Sa Scientific, Inc.’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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Sa Scientific, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?