2026年9月1日，全球医疗科技巨头美敦力与中国腔镜手术机器人企业康诺思腾正式官宣达成深度战略合作。
近日，南京山海医疗科技有限公司“刺激记录电极”获批国家药监局第三类医疗器械注册（注册证编号国械注准20263071824）
8月31日，《深圳经济特区促进脑机接口产业创新发展若干规定（征求意见稿）》正式发布，面向社会公开征求意见。
At the Medical‑Health Pavilion of the Changping‑Future Science City exhibition group, Chunfeng Huayu (Beijing) Intelligent Medical Technology Co., Ltd. showcased its self‑developed world‑first three‑arm surgical robot. Boasting its groundbreaking human‑shaped three‑arm architecture and end‑to‑end in
在昌平·未来科学城展团的医药健康展区，春风化雨（北京）智能医疗科技有限公司携其自主研发的全球首创三臂手术机器人亮相，凭借突破性的人形三臂架构与全链条智能手术能力，迅速引发行业广泛关注。
On August 7, 2026, Intuitive Surgical’s gastrointestinal endoscopic robot, the IG1000, secured FDA 510(k) clearance under clearance number K253702.
2026年8月7日直观外科旗下消化内镜机器人IG1000正式获得FDA 510(k)批准上市，510(k)编号为K253702。
8月26日，美国脑机接口企业 Paradromics 宣布，其研发中的侵入式脑机接口系统 Connexus®获得美国食品药品监督管理局（FDA）批准，可在 Connect-One临床研究中扩展连接更多个人计算设备
Within an implantable‑BCI system, electrodes are responsible for capturing neural signals and chips execute signal‑processing computations. The hermetic feedthrough, by contrast, serves as the critical gateway for signals to pass through the sealed housing of the implanted device.
在植入式脑机接口整机系统中，电极负责拾取神经信号，芯片完成信号处理运算，而气密馈通（Hermetic Feedthrough）则是信号穿越植入设备密封外壳的核心关口。
On August 27, 2026, Apollomics (688176.SH) officially announced that its independently‑developed portable single‑use flexible blue‑light cystoscope, APLD‑2304, has successfully obtained CE certification under the EU Medical Device Regulation (MDR), alongside an ISO 13485:2016 Quality Management Syst
2026年8月27日，亚虹医药（688176.SH）正式宣布，其自主研发的便携式一次性蓝光膀胱软镜APLD-2304，已顺利获得欧盟医疗器械法规（MDR）CE认证，同步取得ISO 13485:2016质量管理体系证书。
Recently, a domestic‑developed laparoscopic surgical robot has achieved a landmark breakthrough in core‑technology dimensions.
近日国产腔镜手术机器人在核心技术维度实现重大里程碑突破。
On August 25, Lepu Medical (300003.SZ) released its investor‑relations activity record, disclosing that the company’s interventional multi‑channel brain‑computer‑interface (BCI) product has successfully completed animal experiments and officially entered the human‑subject Investigator‑Initiated Tria
8 月 25 日，乐普医疗（300003.SZ）披露投资者关系活动记录，公司介入型多通道脑机接口产品已顺利完成动物实验，正式进入人体 IIT 研究者发起临床研究阶段
According to a recent announcement on GeRay‑Tech’s official WeChat account, its Newton‑Endo series minimally‑invasive spinal endoscopic surgical robot has successfully completed the world’s first in‑vivo animal experiment with autonomous robotic operation, under the full‑process witness of the team
近日歌锐科技官微显示，其“牛顿Endo”系列脊柱内镜微创手术机器人，在中国人民解放军总医院（301医院）丁宇主任团队的全程见证下，顺利完成全球首次脊柱内镜机器人自主操作活体动物实验。
Recently, the U.S. Food and Drug Administration (FDA) has granted commercialization authorization for Aletta, a fully‑autonomous blood‑collection robot developed by Dutch medical‑robotics firm Vitestro, via the De Novo classification pathway for innovative medical devices.
近日，美国食品药品监督管理局（FDA）通过De Novo创新器械路径，正式授权荷兰医疗机器人公司Vitestro研发的全自主采血机器人Aletta上市。
