FDA applicant

Ibramed Equipamentos Medicos

Aventura, FL7 decisions2012–20250 recalls

FDA records 7 decisions for Ibramed Equipamentos Medicos (Aventura, FL) from 2012 to 2025: 7 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Its devices cite 11 predicates, 3 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Ibramed Equipamentos Médicos”.

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 Ibramed Equipamentos Medicos’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2012high 3 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Ibramed Equipamentos Medicos by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

See the 510(k) Report

Other applicant names beginning “Ibramed”

FDA records each applicant name separately; these may or may not be the same firm.

Ibramed- Industria Brazileria DE Equipamentos Medi 1

Ibramed Equipamentos Medicos

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?

Other applicant names beginning “Ibramed”