FDA applicant

Synbiotics Corp.

San Diego, CA3 decisions1986–19880 recalls

FDA records 3 decisions for Synbiotics Corp. (San Diego, CA) from 1986 to 1988: 3 510(k) clearances. Most are in product codes LJP (Antiserum, Fluorescent, Chlamydia Trachomatis) and GTZ (Antisera, All Groups, Streptococcus Spp.). 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, microbiology panel, where it files most

How often FDA has decided Synbiotics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Synbiotics Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Synbiotics Corp.’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

Synbiotics Corp.

Which product codes does it file in?

What has FDA decided for it lately?