FDA applicant

Carmel Medical Devices

Carmel, CA1 decision1985–19850 recalls

FDA records 1 decision for Carmel Medical Devices (Carmel, CA) in 1985: 1 510(k) clearance. All are in product code BTR (Tube, Tracheal (W/Wo Connector)). 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 Carmel Medical Devices’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Carmel Medical Devices since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Carmel”

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

Carmel Pharma Ab. 7

Carmel Medical Devices

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Carmel”