FDA applicant

Ri Mos. S.R.L.

Concord, MA4 decisions1999–19990 recalls

FDA records 4 decisions for Ri Mos. S.R.L. (Concord, MA) in 1999: 4 510(k) clearances. Most are in product codes HHK (Curette, Suction, Endometrial (And Accessories)) and HIB (Speculum, Vaginal, Nonmetal). Its devices cite 2 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Ri Mos. S.R.L. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ri Mos. S.R.L. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Ri Mos. S.R.L.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?