FDA applicant

Metric Medical Devices, Inc.

Helotes, TX3 decisions2013–20240 recalls

FDA records 3 decisions for Metric Medical Devices, Inc. (Helotes, TX) from 2013 to 2024: 3 510(k) clearances. Most are in product codes JDR (Staple, Fixation, Bone) and KTT (Appliance, Fixation, Nail/Blade/Plate…). Its devices cite 4 predicates, 1 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 Metric Medical Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Metric Medical Devices, Inc. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Metric Medical Devices, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Metric Medical Devices, Inc.

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?