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Incompass Total Ankle System

FDA UDI

Class II (US FDA UDI)

by Wright Medical Technology, Inc.

Identity

Trade Name
Incompass Total Ankle System FDA UDI
Generic Name
Fixed-bearing total ankle prosthesis FDA UDI
Device Name
Poly FDA UDI
Model / Reference
33855508 FDA UDI
Description
Poly FDA UDI

Identifiers

Catalog Number
33855508 FDA UDI
Primary DI / UDI-DI
00889797114769 FDA UDI
FDA Product Code
HSN FDA UDI
GMDN Term
Fixed-bearing total ankle prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3110 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

Dimensions & Sizes

Size
Height — 8 Millimeter FDA UDI

Category: Fixed-bearing total ankle prosthesis

Incompass Total Ankle System by Wright Medical Technology, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fixed-bearing total ankle prosthesis.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 31c4792e-1baa-4467-9677-cbc9513b2894 36 fields · synced Jun 8, 2026