510(k) Report

FDA applicant

Maternus, Inc.

San Antonio, TX3 decisions2001–20040 recalls

FDA records 3 decisions for Maternus, Inc. (San Antonio, TX) from 2001 to 2004: 3 510(k) clearances. All are in product code HFW (Clamp, Umbilical). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Maternus, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Maternus, 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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Which product codes does it file in?

  • HFWClamp, Umbilical3decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K011621Koala Clamp, Koala Clamp and CutterMaternus, Inc. · 20011cites it

What has FDA decided for it lately?

  • K041332Joey Clamp Opening ToolMaternus, Inc. · 2004
  • K011621Koala Clamp, Koala Clamp and CutterMaternus, Inc. · 2001
  • K010695Koala ClampMaternus, Inc. · 2001

All 3 as Maternus, Inc. →