FDA Device Establishments · JSON-LD · Markdown
FEI 3010677917 · Manufacture Medical Device · Status: Active
| FEI Number | 3010677917 |
|---|---|
| Owner / Operator | Shenzhen Goodwind Technology Development CO., LTD (#10046014) |
| Address | Room 801, Building 1, Baolong Intelligent Manufacturing Park, No. 34, Baotong Road, Baolong Community,, Baolong Street, Longgang District, Shenzhen, P.R. China, Shezhen Guangdong, 518116, CN |
| Mandatory US Agent | Simply Shipped, LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OHS |
| Regulation § (21 CFR) | 878.4810 |
| Proprietary names | Eye Recovery Pro (PH-e03) |
Source: openFDA. Public-domain (CC0).