Flow-Nail™

FDA UDI

Class II (US FDA UDI)

by Flow-Fx, LLC

Identity

Trade Name: Flow-Nail™ FDA UDI
Generic Name: Orthopaedic trocar blade, reusable FDA UDI
Device Name: FN CORT Sheath Trocar FDA UDI
Model / Reference: 101-61 FDA UDI
Description: FN CORT Sheath Trocar FDA UDI

Identifiers

Catalog Number: 101-61 FDA UDI
Primary DI / UDI-DI: B267101610 FDA UDI
510(k) Number: K140601 FDA UDI
FDA Product Code: DRC FDA UDI
GMDN Term: Orthopaedic trocar blade, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.1390 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic trocar blade, reusable

Flow-Nail™ by Flow-Fx, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K140601 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Flow-Fx, LLC

Sources (1)

FDA UDI b2e2baa5-fd1b-412d-acae-43d30fc51228 35 fields · synced Jun 7, 2026