FDA Device Establishments · JSON-LD · Markdown
FEI 3019585045 · Manufacture Medical Device · Status: Active
| FEI Number | 3019585045 |
|---|---|
| Owner / Operator | Prollenium Medical Technologies Inc. (#10055618) |
| Address | 29 East Wilmot Street, Richmond Hill Ontario, L4B1A3, CA |
| Mandatory US Agent | Emergo Global Representation LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LMH |
| Proprietary names | Revanesse Versa; Revanesse Versa+ with Lidocaine; Revanesse® Lips + with Lidocaine; Revanesse Versa+ with Lidocaine 1.2 mL; Revanesse® Versa 1.2 mL; Revanesse® Lips + with Lidocaine 1.2 mL |
Source: openFDA. Public-domain (CC0).