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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
Phalangeal joint arthrodesis implant FDA UDI
Model / Reference
45763516 FDA UDI

Identifiers

Catalog Number
45763516 FDA UDI
Primary DI / UDI-DI
00840420123145 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Phalangeal joint arthrodesis implant 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 16 Millimeter FDA UDI
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Phalangeal joint arthrodesis implant

A comprehensive medical device directory listing the PRO-TOE device, including its specifications, features, and usage. The PRO-TOE device is a small, non-bioabsorbable implantable device used for phalangeal joint arthrodesis, typically in patients with arthritis or deformities.

Similar devices

Also classified as Phalangeal joint arthrodesis implant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wright Medical Technology, Inc.

Sources (1)

  • FDA UDI 77729e79-9b5f-4622-ad39-62824c94fc48 35 fields · synced Jul 11, 2026