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Alliance

FDA UDI

Class II (US FDA UDI)

by Zimmer, Inc.

Identity

Trade Name
Alliance FDA UDI
Generic Name
Glenoid orthopaedic reamer FDA UDI
Model / Reference
110040439 FDA UDI

Identifiers

Primary DI / UDI-DI
00889024682016 FDA UDI
510(k) Number
K233148 FDA UDI
K241043 FDA UDI
FDA Product Code
KWT FDA UDI
PHX FDA UDI
KWS FDA UDI
GMDN Term
Glenoid orthopaedic reamer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3650 FDA UDI
888.3660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Glenoid orthopaedic reamer

Alliance by Zimmer, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glenoid orthopaedic reamer.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zimmer, Inc.

Sources (1)

  • FDA UDI d3fc6b27-87e9-4c53-9515-a47d11a965ee 34 fields · synced May 30, 2026