Ibramed Equipamentos Medicos
Aventura, FL, US
Ibramed Equipamentos Medicos appears in FDA device records in Aventura, FL. FDA records list 7 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 7
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 7 510(k) clearances for Ibramed Equipamentos Medicos between 2012 and 2025. The busiest year on record is 2014, with 3. The most recent is 2025, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2012 | 1 |
| 2013 | 1 |
| 2014 | 3 |
| 2021 | 1 |
| 2025 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K242859 | VEGA | GEX | Substantially Equivalent | |
| K210572 | Neurodyn V2.0, Neurodyn Aussie V2.0 | IPF | Substantially Equivalent | |
| K131926 | THERMOPULSE | IMJ | Substantially Equivalent | |
| K131917 | NEURODYN COMPACT, NEURODYN II | IPF | Substantially Equivalent | |
| K131309 | SONOPULSE COMPACT 1MHZ, SONOPULSE COMPACT 3MHZ | IMI | Substantially Equivalent | |
| K131629 | NEURODYN MULTIWAVE, AUSSIE SPORT | IPF | Substantially Equivalent | |
| K121369 | NEURODYN RUBY MUSCLE STIMULATOR, NEURODYN AUSSIE MUSCLE STIMULATOR | GZJ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain