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Toe MotionTM

FDA UDI

Class U (US FDA UDI)

by Arthrosurface Incorporated

Identity

Trade Name
Toe MotionTM FDA UDI
Generic Name
Total metatarsophalangeal joint prosthesis, modular FDA UDI
Device Name
Insert Delivery Tool, DF-P FDA UDI
Model / Reference
9P15-0100 FDA UDI
Description
Insert Delivery Tool, DF-P FDA UDI

Identifiers

Catalog Number
9P15-0100 FDA UDI
Primary DI / UDI-DI
M5289P1501000 FDA UDI
510(k) Number
K132496 FDA UDI
FDA Product Code
LZJ FDA UDI
GMDN Term
Total metatarsophalangeal joint prosthesis, modular FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Category: Total metatarsophalangeal joint prosthesis, modular

Toe MotionTM by Arthrosurface Incorporated — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total metatarsophalangeal joint prosthesis, modular.

Cleared under the same submission

K132496 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Arthrosurface Incorporated

Sources (1)

  • FDA UDI ad9c5ddd-b446-4b39-98b2-0351acf0dfc1 36 fields · synced May 30, 2026