FDA Device Establishments · JSON-LD · Markdown
FEI 1000135961 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 1000135961 |
|---|---|
| Owner / Operator | BOLTON MEDICAL, INC. (#9007572) |
| Address | 799 International Pkwy, Sunrise, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MIH |
| Proprietary names | TREOFit Template; TREO AUI Stent-Graft System; Relay Thoracic Stent-Graft with Transport Delivery System; TREO Occluder System; TREO Abdominal Stent-Graft System; Relay NBS Plus Stent -Graft System; Relay Plus Thoracic Stent-Graft System; RelayPro Thoracic Stent Graft System |
Source: openFDA. Public-domain (CC0).