FDA Device Establishments · JSON-LD · Markdown
FEI 3015588280 · Manufacture Medical Device Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3015588280 |
|---|---|
| Owner / Operator | SUBLIMED (#10088953) |
| Address | 137 Rue Mayoussard, Moirans Auvergne-Rhone-Alpes, 38380, FR |
| Mandatory US Agent | Medical Device Academy Incorporated |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 5 |
| Product codes (top 20) | NYN, GZJ, IPF, NGX, NUH |
| Regulation § (21 CFR) | 882.5890, 890.5850 |
| Proprietary names | actiTENS Android app; actiTENS mini KIT; actiTENS iOs app; actiTENS mini Textile Accessory; actiTENS mini spare |
Source: openFDA. Public-domain (CC0).