Clearance Summary
Redermo Wound Matrix received FDA 510(k) clearance under submission number K260020, sponsored by Beijing Kreate Medical Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 2026-04-16.
- Submission: K260020
- Applicant / Sponsor: Beijing Kreate Medical Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Unknown
- Device class:
- Decision date: 2026-04-16
Classification & Regulation
This clearance is catalogued under FDA product code QSZ , within the Unknown review panel as a device.