K253999
- 510(k) 号
- K253999
- 器械名称
- Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic Screw
- 申请人
- Nobel Biocare AB SE
- 产品代码
- NHA — Abutment, Implant, Dental, Endosseous
- 批准日期
- 2026-08-06
- 受理日期
- 2025-12-15
- 决定
- Substantially Equivalent
- 审查途径
- Traditional
- 咨询委员会
- Dental
FDA 官方记录: K253999
数据来自 openFDA 510(k) 数据集(CC0 公有领域),以 FDA 现行记录为准。510(k) 许可不等于 FDA 认证或批准。