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Lesser Metatarsal Shortening System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Lesser Metatarsal Shortening System FDA UDI
Generic Name
Orthopaedic bone wire FDA UDI
Device Name
Met Shortening Pilot Hole Wire, 2.25 FDA UDI
Model / Reference
P35-940-0225 FDA UDI
Description
Met Shortening Pilot Hole Wire, 2.25 FDA UDI

Identifiers

Catalog Number
P35-940-0225 FDA UDI
Primary DI / UDI-DI
00889795123770 FDA UDI
FDA Product Code
HXI FDA UDI
GMDN Term
Orthopaedic bone wire FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bone wire

Lesser Metatarsal Shortening System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone wire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 183093fb-ff89-4775-9dd5-43f978d8ed72 34 fields · synced Jun 8, 2026