FDA applicant

Microvas Systems, Inc.

San Antonio, TX1 decision1997–19970 recalls

FDA records 1 decision for Microvas Systems, Inc. (San Antonio, TX) in 1997: 1 510(k) clearance. All are in product code IPF (Stimulator, Muscle, Powered). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Microvas Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Microvas Systems, 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

Microvas Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?