Alteon

FDA UDI

Class II (US FDA UDI)

by Exactech, Inc.

Identity

Trade Name: Alteon FDA UDI
Generic Name: Press-fit femoral stem prosthesis FDA UDI
Model / Reference: 188-00-12 FDA UDI

Identifiers

Catalog Number: 188-00-12 FDA UDI
Primary DI / UDI-DI: 10885862250841 FDA UDI
510(k) Number: K140674 FDA UDI
FDA Product Code: MEH FDA UDI
LZO FDA UDI
LWJ FDA UDI
LPH FDA UDI
KWZ FDA UDI
KWY FDA UDI
JDI FDA UDI
GMDN Term: Press-fit femoral stem prosthesis FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3353 FDA UDI
888.3360 FDA UDI
888.3358 FDA UDI
888.3310 FDA UDI
888.3390 FDA UDI
888.3350 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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Press-fit femoral stem prosthesis

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

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OrthoMedFlex — ORTHOMEDFLEX LLC · Class II
BI-METRIC X-SERIES HIP SYSTEM — Biomet Orthopedics, Inc. · Class II
Accolade — Howmedica Osteonics Corp. · Class II
BI-METRIC HIP SYSTEM — Biomet Orthopedics, Inc. · Class II

Cleared under the same submission

K140674 also covers:

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: Exactech, Inc.

Sources (1)

FDA UDI 5684c10a-ebdc-4090-ae0d-aeaa45e35c95 35 fields · synced Jun 1, 2026