510(k) Report

FDA applicant

The Orthopaedic Implant Company (Oic)

Reno, NV1 decision2013–20130 recalls

FDA records 1 decision for The Orthopaedic Implant Company (Oic) (Reno, NV) in 2013: 1 510(k) clearance. All are in product code HRS (Plate, Fixation, Bone). 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 The Orthopaedic Implant Company (Oic)’s devices, and how often a recall has named them.

FDA decisions per year

1in 2013

2013: 1
2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — The Orthopaedic Implant Company (Oic) by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • HRSPlate, Fixation, Bone1decision

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.

  • K123832Oic Distal Radius Plating System, Oic Proximal Humerus Plating System, Oic Clavicle Plating System, the Oic…The Orthopaedic Implant Company (Oic) · 20132cite it

What has FDA decided for it lately?

  • K123832Oic Distal Radius Plating System, Oic Proximal Humerus Plating System, Oic Clavicle Plating System, the Oic…The Orthopaedic Implant Company (Oic) · 2013

The one decision as The Orthopaedic Implant Company (Oic) →