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Memo 4D Curve 4DC30

by Corcym Inc.

Memo 4D Curve 4DC30 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 08022057015983), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K261707

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08022057015983 UDI-DI Date4 Jul 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Special NumberK261707 Date18 Jun 2026DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K261707 decided 18 Jun 2026 Active
  • FDA GUDID UDI-DI 08022057015983 listed 4 Jul 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K261707
  2. Listed FDA GUDID 08022057015983

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Memo 4D Curve
Generic name
Mitral/tricuspid annuloplasty ring, open-surgery
Model / Ref / Catalog
4DC30
Primary DI / UDI-DI
08022057015983
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

Other devices from Corcym Inc.

  • TriMemo TRIM-26

    Class II
  • TriMemo TRIM-28

    Class II
  • TriMemo TRIM-30

    Class II
  • TriMemo TRIM-32

    Class II

See all devices from Corcym Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Serial number
  • Expiration date
Other properties (9, all answered No)