FDA applicant

Camino Laboratories, Inc.

San Diego, CA18 decisions1982–19950 recalls

FDA records 18 decisions for Camino Laboratories, Inc. (San Diego, CA) from 1982 to 1995: 18 510(k) clearances. Most are in product codes DXO (Transducer, Pressure, Catheter Tip) and GWM (Device, Monitoring, Intracranial Pressure). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Camino Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Camino Laboratories, 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 “Camino”

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

Camino Neurocare, Inc. 3

Camino Laboratories, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Camino”