510(k) Report

FDA applicant

Minumys Surgical, Inc.

Cupertino, CA1 decision1999–19990 recalls

FDA records 1 decision for Minumys Surgical, Inc. (Cupertino, CA) in 1999: 1 510(k) clearance. All are in product code DXC (Clamp, Vascular). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Minumys Surgical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Minumys Surgical, 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