Data / Medical devices / Brazil / Avanutri Equipamentos De Saude Ltda
Avanutri Equipamentos De Saude Ltda: FDA-registered device maker in Tres Rios Rio de Janeiro, Brazil, 1 510(k) clearance
Avanutri Equipamentos De Saude Ltda is registered with the FDA (registration 3035374320) in Tres Rios Rio de Janeiro, Brazil. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 29, 2026. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3035374320
- Address
- Rua SANTO ANTONIO 2262, Tres Rios Rio de Janeiro, Brazil, 25820-185
- Owner or operator
- AVANUTRI EQUIPAMENTOS DE SAUDE LTDA (10092515)
- Roles
- Manufacturer
- First device listed
- January 16, 2025
- Registered through
- 2026
- Brand names listed
- AVA BOOTS 5, Cryo Sport 2, DeepLed, LedBoots
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Massager, Powered Inflatable Tube | IRP | 2 | Manufacturer | accessdata.fda.gov |
| Pack, Hot Or Cold, Water Circulating | ILO | 2 | Manufacturer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 29, 2026 | K252396 | Cryo Sport 2.0 (AVA 501) | IRP | Substantially Equivalent | Avanutri Equipamentos DE Saúde | accessdata.fda.gov |
Compare with other makers
- All makers of Vibrator, Therapeutic
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Pack, Hot Or Cold, Water Circulating
- All makers of Massager, Powered Inflatable Tube
Updated May 29, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.