Memo 4D Curve 4DC34
by Corcym Inc.
Memo 4D Curve 4DC34 is a Class II device made by Corcym Inc., cleared under FDA 510(k) K261707 on 18 Jun 2026 and listed in FDA GUDID since 4 Jul 2026 (UDI-DI 08022057016003), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08022057016003 | Date4 Jul 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK261707 | Date18 Jun 2026 | StatusActive |
Official records
- AccessGUDID record 08022057016003
- FDA 510(k) database K261707
Across registries
- FDA 510(k) K261707 decided 18 Jun 2026 Active
- FDA GUDID UDI-DI 08022057016003 listed 4 Jul 2026 Listed
Timeline
- Cleared FDA 510(k) K261707
- Listed FDA GUDID 08022057016003
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Memo 4D Curve
- Generic name
- Mitral/tricuspid annuloplasty ring, open-surgery
- Model / Ref / Catalog
- 4DC34
- Primary DI / UDI-DI
- 08022057016003
- 510(k) Number
- FDA product code
- KRH
- GMDN term
- Mitral/tricuspid annuloplasty ring, open-surgery
- Device class
- Class II
- Regulation number
- 870.3800
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional