FDA Device Establishments · JSON-LD · Markdown
FEI 3012867029 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3012867029 |
|---|---|
| Owner / Operator | Orbray Co., Ltd. (#10053339) |
| Address | 3-8-22 Shinden Adachi Ku, Tokyo, 1238511, JP |
| Mandatory US Agent | Pro Pharma Group |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EIH |
| Regulation § (21 CFR) | 872.6660 |
| Proprietary names | LayZir Disc; Zirconia Disc; SHOFU DISK ZR Lucent Supra |
Source: openFDA. Public-domain (CC0).