FDA applicant

Camino Neurocare, Inc.

San Diego, CA3 decisions1996–19982 recalls

FDA records 3 decisions for Camino Neurocare, Inc. (San Diego, CA) from 1996 to 1998: 3 510(k) clearances. All are in product code GWM (Device, Monitoring, Intracranial Pressure). Its devices cite 5 predicates, 0 of them its own earlier devices. 2 recalls are 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 Neurocare, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

1in 2013

2007high 1 (2011) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Camino Neurocare, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Camino”

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

Camino Laboratories, Inc. 18

Camino Neurocare, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Camino”