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Phalinx

FDA UDI

Class II (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
PHALINX FDA UDI
Generic Name
Phalangeal joint arthrodesis implant FDA UDI
Model / Reference
45301002 FDA UDI

Identifiers

Catalog Number
45301002 FDA UDI
Primary DI / UDI-DI
00840420166036 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

Category: Phalangeal joint arthrodesis implant

The PHALINX medical device is a non-surgical solution for managing arthritis and deformities in the finger and/or toe. It's a small, implantable device that fuses joint structures, typically used after orthopedic surgery or as a revision procedure.

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 dcc1c29b-dc4a-459e-bdf3-4c66290219f0 35 fields · synced Jul 11, 2026