Stride

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: STRIDE FDA UDI
Generic Name: Unicondylar knee insert FDA UDI
Device Name: Stride Poly Insert Size C 8mm FDA UDI
Model / Reference: PFSI00033 FDA UDI
Description: Stride Poly Insert Size C 8mm FDA UDI

Identifiers

Catalog Number: PFSI00033 FDA UDI
Primary DI / UDI-DI: 00885556626979 FDA UDI
FDA Product Code: HSX FDA UDI
GMDN Term: Unicondylar knee insert FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3520 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Unicondylar knee insert

Stride by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Unicondylar knee insert.

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Vivacit-E® — Zimmer, Inc. · Class II
Unicondylar Knee System — GLOBUS MEDICAL, INC. · Class II
MOTO Partial Knee System - Medial — Medacta International · Class II
GMK Uni — Medacta International · Class II
SIGMA — DEPUY (IRELAND) · Class II
MOTO Partial Knee System — Medacta International · Class II
iDuo® iPoly™ Insert Kit — Conformis, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI c3c108d5-6c86-47ba-b391-36b8d2f95ced 35 fields · synced Jun 8, 2026