ANEUVO
Matched from indexed company URL: Aneuvo
FDA Registration(s)
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|
| | ANEUVO | 5 | N | 2026-01-01 | 10940 Wilshire Blvd Ste 2030 Los Angeles CA US 90024 |
Registered Device Listings
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|
| 350439 | 1553009590 | K252893 | ExaStim® Stimulation System (EXA-001); ExaStim® Stimulation System (EXA-011); ReCure® Electrode Pad (PAD-003); ReCure® Electrode Pad (PAD-013) | SDO | 2026-03-27 |
Product Codes Associated With Registrations
| Product code | Registration listing records | Latest decision |
|---|
| SDO | 1 | 2026-03-27 |