510(k) Report

FDA applicant

Creative Biomedics, Inc.

San Clemente, CA4 decisions1995–19970 recalls

FDA records 4 decisions for Creative Biomedics, Inc. (San Clemente, CA) from 1995 to 1997: 4 510(k) clearances. Most are in product codes BZC (Calculator, Pulmonary Function Data) and CAH (Filter, Bacterial, Breathing-Circuit). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Creative Biomedics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Creative Biomedics, 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 “Creative”

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