FDA applicant

Biomed Diagnostics, Inc.

San Jose, CA3 decisions1990–20210 recalls

FDA records 3 decisions for Biomed Diagnostics, Inc. (San Jose, CA) from 1990 to 2021: 3 510(k) clearances. Most are in product codes JTY (Culture Media, For Isolation Of Pathogenic…) and JSN (Culture Media, Propagating Transport). Its devices cite 1 predicate, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Biomed Diagnostics Incorporated”.

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 Biomed Diagnostics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2007high 1 (2021) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Biomed Diagnostics, 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 “Biomed”

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

Biomed Devices Corp. 2 The Biomed Group 2 Biomed Personal Metabolic and Nutritional Testing 2 Biomed Laboratories, Inc. 1 Biomed Ent, Inc. 1 Biomed Products 1

Biomed Diagnostics, Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Biomed”