FDA applicant

Innerspace Medical, Inc.

Irvine, CA1 decision1994–19940 recalls

FDA records 1 decision for Innerspace Medical, Inc. (Irvine, CA) in 1994: 1 510(k) clearance. All are in product code 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 Innerspace Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innerspace Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Innerspace”

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

Innerspace, Inc. 8 Innerspace Neuro Solutions, Inc. 1

Innerspace Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Innerspace”