FDA applicant

Menlo Care, Inc.

Menlo Park, CA31 decisions1986–19970 recalls

FDA records 31 decisions for Menlo Care, Inc. (Menlo Park, CA) from 1986 to 1997: 31 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and DYB (Introducer, Catheter). Its devices cite 1 predicate, 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Menlo Care, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Menlo”

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

Menlo Brands, LLC 1

Menlo Care, 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 “Menlo”