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HARBOR Occlusion Device
Nuvascular, Inc.
·
,
United States
(FDA applicant)
FDA 510(k)
K260635
Active
Cleared 12 Jun 2026
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Nuva™
Beijing Taijieweiye Technology Co., Ltd.
·
,
China
Group of variants
CE/MDR
MDR 824536
Active
Valid to Jul 2031
Active
Regimes:
CE MDR
Registry:
EUDAMED
Class
Class:
III
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