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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
Carpal scaphoid prosthesis FDA UDI
Model / Reference
482305R FDA UDI

Identifiers

Catalog Number
482305R FDA UDI
Primary DI / UDI-DI
00840420132840 FDA UDI
FDA Product Code
KWO FDA UDI
GMDN Term
Carpal scaphoid prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3760 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

Category: Carpal scaphoid prosthesis

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

Similar devices

Also classified as Carpal scaphoid prosthesis.

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 91e812f7-02ff-4b52-876e-f7d46435127e 35 fields · synced Jun 8, 2026