FDA applicant

21 Equipment S.R.L.

Torino, IT2 decisions2022–20230 recalls

FDA records 2 decisions for 21 Equipment S.R.L. (Torino, IT) from 2022 to 2023: 2 510(k) clearances. Most are in product codes PBX (Massager, Vacuum, Radio Frequency Induced Heat) and NFO (Stimulator, Transcutaneous Electrical…). 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, general and plastic surgery panel, where it files most

How often FDA has decided 21 Equipment S.R.L.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2023

2022high 1 (2022) · low 0 (2024)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — 21 Equipment S.R.L. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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21 Equipment S.R.L.

Which product codes does it file in?

What has FDA decided for it lately?