510(k) Report

FDA applicant

Enovis

Calrsbadd1 decision2025–20250 recalls

FDA records 1 decision for Enovis (Calrsbadd) in 2025: 1 original PMA approval. All are in product code LOF (Stimulator, Bone Growth, Non-Invasive). 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 Enovis’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2025: 1
2025high 1 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2025.

FIG. 1 — Enovis by year, 2025–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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