510(k) Report

FDA applicant

Medmetric Corp.

San Diego, CA8 decisions1980–19950 recalls

FDA records 8 decisions for Medmetric Corp. (San Diego, CA) from 1980 to 1995: 8 510(k) clearances. Most are in product codes LYH (Arthrometer) and FTY (Tape, Measuring, Rulers And Calipers). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for Medmetric Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medmetric Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medmetric Corp.’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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