Miracu™ Polydioxanone (PDO) Suture and Needle (MONO)

FDA 510(k)

Class II (US FDA 510(k))

510(k) K251414

Identifiers

510(k) Number: K251414 FDA 510(k)
FDA Product Code: NEW FDA 510(k)

Classification

Device Class: Class II FDA 510(k)
Legislation / Framework: 21 CFR Part 878.4840 FDA 510(k)
Regulation Number: 878.4840 FDA 510(k)
Advisory Committee: General, Plastic Surgery FDA 510(k)
FDA Decision: SESE Substantially Equivalent FDA 510(k)

Miracu™ Polydioxanone (PDO) Suture and Needle (MONO) by Feeltech Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Source	Region	Type	Cert / Approval No.	Class	Status
FDA 510(k)	United States	FDA_510K	K251414	Class II	Active

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Manufacturer

Manufacturer: Feeltech Co., Ltd.

Sources (1)

FDA 510(k) K251414 24 fields · synced Jun 18, 2026