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Flow-Nail™

FDA UDI

Class II (US FDA UDI)

by Flow-Fx, LLC

Identity

Trade Name
Flow-Nail™ FDA UDI
Generic Name
Orthopaedic coaxial injection applicator FDA UDI
Device Name
FN BVF Plunger FDA UDI
Model / Reference
101-72 FDA UDI
Description
FN BVF Plunger FDA UDI

Identifiers

Catalog Number
101-72 FDA UDI
Primary DI / UDI-DI
B267101720 FDA UDI
510(k) Number
K140601 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic coaxial injection applicator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic coaxial injection applicator

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

Similar devices

Also classified as Orthopaedic coaxial injection applicator.

Cleared under the same submission

K140601 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Flow-Fx, LLC

Sources (1)

  • FDA UDI 6e9b185b-743a-46d1-a723-81bc1da6dd3d 35 fields · synced May 31, 2026