Identity
- Trade Name
- Alteon FDA UDI
- Generic Name
- Orthopaedic broach FDA UDI
- Device Name
- ALT HA L COMP BRCH SZ 2 FDA UDI
- Model / Reference
- 191-02-02 FDA UDI
- Description
- ALT HA L COMP BRCH SZ 2 FDA UDI
Identifiers
- Catalog Number
- 191-02-02 FDA UDI
- Primary DI / UDI-DI
- 10885862513649 FDA UDI
- FDA Product Code
- KWY FDA UDIMEH FDA UDIKWL FDA UDIKWZ FDA UDILZO FDA UDILWJ FDA UDI
- GMDN Term
- Orthopaedic broach FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3390 FDA UDI888.3353 FDA UDI888.3360 FDA UDI888.3310 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic broach
Alteon by Exactech, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic broach.
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Cleared under the same submission
K162732 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Exactech, Inc.
Sources (1)
- FDA UDI b989461e-6620-4290-8f80-cefb5e00cf27 36 fields · synced May 30, 2026