FDA Device Establishments · JSON-LD · Markdown
FEI 3002807826 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3002807826 |
|---|---|
| Owner / Operator | SYBRON DENTAL SPECIALTIES, INC. (#9029565) |
| Address | CALLE 21, No. 1103, AMPLIACION, CIUDAD IND., YUCATAN UMAN, 97390, MX |
| Mandatory US Agent | Sybron Dental Specialties Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EKM |
| Regulation § (21 CFR) | 872.3850 |
| Proprietary names | Elements Gutta Percha Cartridge; K3XF Gutta Percha; SoftCore; TF Adaptive Gutta Percha; TF Adaptive Obturator; Gutta Percha Cartridge; TF Adaptive Verifiers; Gutta Percha; Zenflex Pre-Tip Gutta Percha; Autofit Gutta Percha |
Source: openFDA. Public-domain (CC0).