510(k) Report

FDA applicant

Cm Technologies, Inc.

San Diego, CA2 decisions2021–20260 recalls

FDA records 2 decisions for Cm Technologies, Inc. (San Diego, CA) from 2021 to 2026: 1 510(k) clearance and 1 De Novo grant. Most are in product codes KNT (Tubes, Gastrointestinal (And Accessories)) and SJB (Powered Fecal Management System). Its devices cite 1 predicate, 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

1in 2021

2021: 12026 (partial year): 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Cm Technologies, Inc. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cm Technologies, 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?

  • KNTTubes, Gastrointestinal (And Accessories)1decision
  • SJBPowered Fecal Management System1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • DEN250043Qoramatic Automated Stool ManagementCm Technologies, Inc. · 2026
  • K212444Qora Stool Management KitCm Technologies, Inc. · 2021

All 2 as Cm Technologies, Inc. →