FDA Device Establishments · JSON-LD · Markdown
FEI 3004730368 · Manufacture Medical Device · Status: Active
| FEI Number | 3004730368 |
|---|---|
| Owner / Operator | NEOBIOTECH CO., LTD. (#9066035) |
| Address | 70, Sinpyeong-ro, Jijeong-myeon, Wonju-si Gangwon, 26351, KR |
| Mandatory US Agent | Withus Group Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NDP |
| Regulation § (21 CFR) | 872.3980 |
| Proprietary names | Scan Bar Screw; Digital Lab Analog Set; Reverse Scan Body; ALX-BT Lab Analog; Neo PickCap Impression KIT; Prosthesis KIT; Prosthetic Planning KIT; Universal Prosthetic KIT; Pick Cap Impression Body; FR Screw Hex Driver |
Source: openFDA. Public-domain (CC0).