Advance®

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name: ADVANCE® FDA UDI
Generic Name: Polyethylene patella prosthesis FDA UDI
Device Name: ADVANCE® ONLAY METAL BACK PATELLA 29MM FDA UDI
Model / Reference: KPON29MB FDA UDI
Description: ADVANCE® ONLAY METAL BACK PATELLA 29MM FDA UDI

Identifiers

Catalog Number: KPON29MB FDA UDI
Primary DI / UDI-DI: M684KPON29MB1 FDA UDI
FDA Product Code: MBH FDA UDI
JWH FDA UDI
GMDN Term: Polyethylene patella prosthesis FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3565 FDA UDI
888.3560 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

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 29 Millimeter FDA UDI

Category: Polyethylene patella prosthesis

Advance® by MicroPort Orthopedics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyethylene patella prosthesis.

VANGUARD KNEE SYSTEM — Biomet Orthopedics, Inc. · Class II
Duracon — Howmedica Osteonics Corp. · Class II
PERSONA® — Zimmer, Inc. · Class II
S-ROM NOILES — DEPUY (IRELAND) · Class II
LOSPA Total Knee System — Corentec Co., Ltd · Class II
Unity Total Knee System — CORIN LTD · Class II
Proven Gen-Flex PS Knee System — GLOBUS MEDICAL, INC. · Class II
LEGION — Smith & Nephew, 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: MicroPort Orthopedics Inc.

Sources (1)

FDA UDI 65be222f-50cb-4980-9358-584313ee0863 36 fields · synced Jun 9, 2026