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Pro-Toe

FDA UDI

Class II (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
PRO-TOE FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
VO Blade FDA UDI
Model / Reference
45712000 FDA UDI
Description
VO Blade FDA UDI

Identifiers

Catalog Number
45712000 FDA UDI
Primary DI / UDI-DI
00840420123022 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2 Millimeter FDA UDI
Length — 13 Millimeter FDA UDI
Angle — 0 degree FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Pro-Toe by Wright Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2364d5ae-f8a1-47da-89b8-af47de7d177a 36 fields · synced Jun 8, 2026