510(k) Report

FDA applicant

C2m Medical, Inc.

San Antonio, TX1 decision2007–20070 recalls

FDA records 1 decision for C2m Medical, Inc. (San Antonio, TX) in 2007: 1 510(k) clearance. All are in product code MBI (Fastener, Fixation, Nondegradable, Soft Tissue). 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, orthopedic panel, where it files most

How often FDA has decided C2m Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — C2m Medical, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MBIFastener, Fixation, Nondegradable, Soft Tissue1decision

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.

  • K073226Cinch Knotless Fixation Implant SystemC2m Medical, Inc. · 20071cites it

What has FDA decided for it lately?

  • K073226Cinch Knotless Fixation Implant SystemC2m Medical, Inc. · 2007

The one decision as C2m Medical, Inc. →