Clearance Summary
Valence InVent Xtend (CVG-4101-VXA) received FDA 510(k) clearance under submission number K253807, sponsored by Convergence Medical Sciences , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2026-08-20.
- Submission: K253807
- Applicant / Sponsor: Convergence Medical Sciences , Ltd.
- Clearance pathway: Traditional
- Review panel: Anesthesiology
- Device class: Class II
- Regulation citation: 21 CFR 868.5895
- Decision date: 2026-08-20
Classification & Regulation
This clearance is catalogued under FDA product code MOD and 21 CFR 868.5895, within the Anesthesiology review panel as a Class II device.