# Ibramed Equipamentos Medicos

- Location (FDA's records): Aventura, FL
- FDA decisions: 7 (2012–2025): 7 510(k) clearances
- Names in FDA's records: Ibramed Equipamentos Medicos (6); Ibramed Equipamentos Médicos (1)
- Product codes: IPF (3), GZJ (1), IMJ (1), IMI (1), GEX (1)
- Predicates its devices cite: 11 (3 its own); citations of its devices by later devices: 6 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Chattanooga Group, Inc.: 3 (https://510kreport.com/company/chattanooga-group)
- Empi: 2 (https://510kreport.com/company/empi)
- Mettler Electronics Corp.: 1 (https://510kreport.com/company/mettler-electronics)
- Lotuxs Medtech (Suzhou) Co., Ltd.: 1 (https://510kreport.com/company/lotuxs-medtech-suzhou)
- Alma Lasers, Inc.: 1 (https://510kreport.com/company/alma-lasers)

## Firms that cite its devices most
- Techlink International: 1 (https://510kreport.com/company/techlink-international)
- Pierenkemper GmbH: 1 (https://510kreport.com/company/pierenkemper)
- Bonutti Research, Inc.: 1 (https://510kreport.com/company/bonutti-research)

## Its most-cited devices
- K121369: Neurodyn Ruby Muscle Stimulator, Neurodyn Aussie Muscle Stimulator (2012), cited by 3
- K131309: Sonopulse Compact 1MHZ, Sonopulse Compact 3MHZ (2014), cited by 1
- K131629: Neurodyn Multiwave, Aussie Sport (2013), cited by 1
- K131917: Neurodyn Compact, Neurodyn II (2014), cited by 1

## Recent decisions
- K242859: VEGA (Sep 19, 2025)
- K210572: Neurodyn V2.0, Neurodyn Aussie V2.0 (May 11, 2021)
- K131926: Thermopulse (Jul 24, 2014)
- K131917: Neurodyn Compact, Neurodyn II (Apr 29, 2014)
- K131309: Sonopulse Compact 1MHZ, Sonopulse Compact 3MHZ (Jan 27, 2014)
- K131629: Neurodyn Multiwave, Aussie Sport (Nov 26, 2013)
- K121369: Neurodyn Ruby Muscle Stimulator, Neurodyn Aussie Muscle Stimulator (Dec 19, 2012)

Source page: https://510kreport.com/company/ibramed-equipamentos-medicos