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FDA 510(k)

MEMO 4D Curve™ Semirigid mitral annuloplasty ring

K-Number: K261707 · 2026-06-18

ApplicantCorcym S.r.l.
Decision Date2026-06-18
Product CodeKRH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEMO 4D Curve™ Semirigid mitral annuloplasty ring is the device name listed in this FDA 510(k) record. The listed applicant is Corcym S.r.l.. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K261707. The device is classified under product code KRH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMO 4D Curve™ Semirigid mitral annuloplasty ring?

MEMO 4D Curve™ Semirigid mitral annuloplasty ring is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is Corcym S.r.l.. The 510(k) number is K261707.

When did MEMO 4D Curve™ Semirigid mitral annuloplasty ring receive FDA 510(k) clearance?

MEMO 4D Curve™ Semirigid mitral annuloplasty ring received FDA 510(k) clearance on 2026-06-18, under 510(k) number K261707.

Who is the listed applicant for MEMO 4D Curve™ Semirigid mitral annuloplasty ring?

The FDA 510(k) record lists Corcym S.r.l. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEMO 4D Curve™ Semirigid mitral annuloplasty ring?

The FDA product code for MEMO 4D Curve™ Semirigid mitral annuloplasty ring is KRH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT04147884A Feasibility Study of the Millipede Transcatheter Annuloplasty Ring System in Patients With Functional Mitral RegurgitationACTIVE_NOT_RECRUITINGNCT04761120Annuloplasty Rings and Band Post-Market Clinical Follow-Up StudyRECRUITING

Other records listing Corcym S.r.l. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

PMA P900060HEART-VALVE, MECHANICALK260498TriMemo™ SEMIRIGID ANNULOPLASTY RINGPMA P150011heart-valve, non-allograft tissueK230318Memo 3D Semirigid Annuloplasty Ring; Memo 3D ReChord Semirigid Annuloplasty Ring; Memo 4D Semirigid Annuloplasty Ring

Related Devices (Code: KRH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260498TriMemo™ SEMIRIGID ANNULOPLASTY RINGCorcym S.r.l.K253232Seguin Annuloplasty RingABBOTT MEDICALK251982Edwards MC3 Tricuspid annuloplasty ring (4900)Edwards Lifesciences, LLCK251688Carpentier-Edwards Physio Annuloplasty Ring (4450)Edwards Lifesciences, LLCK250859TransForm McCarthy Mitral Annuloplasty Ring (TF)Genesee Biomedical, Inc.K232599TransForm McCarthy Mitral Annuloplasty Ring (TF)Genesee Biomedical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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