Identity
- Trade Name
- ADVANCE® FDA UDI
- Generic Name
- Polyethylene patella prosthesis FDA UDI
- Device Name
- ADVANCE® ONLAY ALL-POLY PATELLA 32mm TRI-PEG FDA UDI
- Model / Reference
- KPONTP32 FDA UDI
- Description
- ADVANCE® ONLAY ALL-POLY PATELLA 32mm TRI-PEG FDA UDI
Identifiers
- Catalog Number
- KPONTP32 FDA UDI
- Primary DI / UDI-DI
- M684KPONTP321 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Polyethylene patella prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 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
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
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 32 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- MicroPort Orthopedics Inc.
Sources (1)
- FDA UDI 031d0ef6-01a7-4862-b629-2ea5b7a9ea69 36 fields · synced Jun 9, 2026