FDA Device Establishments · JSON-LD · Markdown
FEI 2518690 · Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device · Status: Active
| FEI Number | 2518690 |
|---|---|
| Owner / Operator | Keystone Industries (#9007845) |
| Address | 2702 Cindel Drive, Unit #2, Cindel Business Park, Delran, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FLG |
| Regulation § (21 CFR) | 880.6150 |
| Proprietary names | Optimize Tartar, Stain & permanent Cement Remover Ultrasonic Liquid; Optimize Refresh Enzymatic Ultrasonic Instrument Cleaner; Optimize Tartar, Stain & Permanent Cement Remover Ultrasonic Powder; Optimize General Purpose Ultrasonic Cleaner-Powder; Optimize General Purpose Ultrasonic Cleaner-Liquid |
Source: openFDA. Public-domain (CC0).