FDA applicant

Osteocentric Technologies D.B.A. Osteocentric Trauma

Logan, UT1 decision2021–20210 recalls

FDA records 1 decision for Osteocentric Technologies D.B.A. Osteocentric Trauma (Logan, UT) in 2021: 1 510(k) clearance. All are in product code JDO (Device, Fixation, Proximal Femoral, Implant). Its devices cite 8 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, orthopedic panel, where it files most

How often FDA has decided Osteocentric Technologies D.B.A. Osteocentric Trauma’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Osteocentric Technologies D.B.A. Osteocentric Trauma by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Osteocentric”

FDA records each applicant name separately; these may or may not be the same firm.

OsteoCentric Technologies 13 Osteocentric Extremities, LLC 1 Osteocentric Trauma 1

Osteocentric Technologies D.B.A. Osteocentric Trauma

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Osteocentric”