FDA applicant

Millennium Biomedical, Inc.

Pomona, CA5 decisions2000–20040 recalls

FDA records 5 decisions for Millennium Biomedical, Inc. (Pomona, CA) from 2000 to 2004: 5 510(k) clearances. All are in product code HNO (Keratome, Ac-Powered). Its devices cite 7 predicates, 0 of them its own earlier devices. 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Millennium Biomedical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Millennium Biomedical, 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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Other applicant names beginning “Millennium”

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

Millennium Dental Technologies, Inc. 5 Millennium Medical Technologies, Inc. 5 Millennium Medical Distribution, Inc. 1 Millennium Medical Technologies Inc (Dba Cellmyx) 1 Millennium Dental International, Inc. 1 Millennium Magnetic Imaging, Inc. 1 Millennium Technology Services 1 Millennium Devices, Inc. 1 Millennium Company, LLC 1

Millennium Biomedical, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Millennium”