FDA Device Establishments · JSON-LD · Markdown
FEI 1000120578 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 1000120578 |
|---|---|
| Owner / Operator | CYNOSURE, LLC (#9006419) |
| Address | 5 CARLISLE RD, Westford, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | GEI |
| Regulation § (21 CFR) | 878.4400 |
| Proprietary names | Acusect, Radiolase II |
Source: openFDA. Public-domain (CC0).