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Advance®

FDA UDI

Class II (US FDA UDI)

by MicroPort Orthopedics Inc.

Identity

Trade Name
ADVANCE® FDA UDI
Generic Name
Uncoated knee tibia prosthesis, metallic FDA UDI
Device Name
ADVANCE® II CoCr TIBIAL BASE NONPOROUS SZ 1+ FDA UDI
Model / Reference
KTCCNP11 FDA UDI
Description
ADVANCE® II CoCr TIBIAL BASE NONPOROUS SZ 1+ FDA UDI

Identifiers

Catalog Number
KTCCNP11 FDA UDI
Primary DI / UDI-DI
M684KTCCNP111 FDA UDI
FDA Product Code
HRY FDA UDI
GMDN Term
Uncoated knee tibia prosthesis, metallic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3530 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

Category: Uncoated knee tibia prosthesis, metallic

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

Similar devices

Also classified as Uncoated knee tibia prosthesis, metallic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MicroPort Orthopedics Inc.

Sources (1)

  • FDA UDI 5446904d-68fa-4104-b11e-65644caa6477 35 fields · synced Jun 9, 2026