510(k) Report

FDA applicant

Conextions Medical

Salt Lake City, UT2 decisions2020–20220 recalls

FDA records 2 decisions for Conextions Medical (Salt Lake City, UT) from 2020 to 2022: 2 510(k) clearances. Most are in product codes GAQ (Suture, Nonabsorbable, Steel, Monofilament And…) and MBI (Fastener, Fixation, Nondegradable, Soft Tissue). Its devices cite 6 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2022

2020: 12022: 1
2020high 1 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Conextions Medical by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GAQSuture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile1decision
  • MBIFastener, Fixation, Nondegradable, Soft Tissue1decision

Whose devices does it build on?

Its devices cite 6 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.

  • K200028Coronet Soft Tissue Fixation SystemConextions Medical · 20201cites it

What has FDA decided for it lately?

  • K203855CoNextions TR Tendon Repair SystemConextions Medical · 2022
  • K200028Coronet Soft Tissue Fixation SystemConextions Medical · 2020

All 2 as Conextions Medical →