510(k) Report

FDA applicant

Centermed, Inc.

Walnut Creek, CA2 decisions2021–20220 recalls

FDA records 2 decisions for Centermed, Inc. (Walnut Creek, CA) from 2021 to 2022: 2 510(k) clearances. Most are in product codes DZJ (Driver, Wire, And Bone Drill, Manual) and PBF (Orthopaedic Surgical Planning And Instrument…). 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, dental panel, where it files most

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

FDA decisions per year

1in 2022

2021: 12022: 1
2021high 1 (2021) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

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

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Which product codes does it file in?

  • DZJDriver, Wire, And Bone Drill, Manual1decision
  • PBFOrthopaedic Surgical Planning And Instrument Guides1decision

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 2 times; 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.

  • K201353CenterMed Patient Matched Assisted Surgical Planning (ASP) SystemCentermed, Inc. · 20211cites it
  • K211614CenterMed Patient Matched Assisted Surgical Planning (ASP) SystemCentermed, Inc. · 20221cites it

What has FDA decided for it lately?

  • K211614CenterMed Patient Matched Assisted Surgical Planning (ASP) SystemCentermed, Inc. · 2022
  • K201353CenterMed Patient Matched Assisted Surgical Planning (ASP) SystemCentermed, Inc. · 2021

All 2 as Centermed, Inc. →