TriMemo™ SEMIRIGID ANNULOPLASTY RING
K-Number: K260498 · 2026-04-14
Device Summary
Frequently Asked Questions
What is the TriMemo™ SEMIRIGID ANNULOPLASTY RING?
TriMemo™ SEMIRIGID ANNULOPLASTY RING is a medical device that received FDA 510(k) clearance on 2026-04-14. The listed applicant is Corcym S.r.l.. The 510(k) number is K260498.
When did TriMemo™ SEMIRIGID ANNULOPLASTY RING receive FDA 510(k) clearance?
TriMemo™ SEMIRIGID ANNULOPLASTY RING received FDA 510(k) clearance on 2026-04-14, under 510(k) number K260498.
Who is the listed applicant for TriMemo™ SEMIRIGID 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 TriMemo™ SEMIRIGID ANNULOPLASTY RING?
The FDA product code for TriMemo™ SEMIRIGID ANNULOPLASTY RING is KRH.
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.
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.
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.