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Swanson

FDA UDI

Class II (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
SWANSON FDA UDI
Generic Name
Total metatarsophalangeal joint prosthesis, one-piece FDA UDI
Model / Reference
4260006 FDA UDI

Identifiers

Catalog Number
4260006 FDA UDI
Primary DI / UDI-DI
00840420121493 FDA UDI
FDA Product Code
KWH FDA UDI
GMDN Term
Total metatarsophalangeal joint prosthesis, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3720 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
MRI Safety
MR Conditional FDA UDI

Category: Total metatarsophalangeal joint prosthesis, one-piece

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

Similar devices

Also classified as Total metatarsophalangeal joint prosthesis, one-piece.

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 3b77df3b-af16-4ef2-92df-bf91fe99c891 35 fields · synced Jun 8, 2026