Identity
- Trade Name
- FuzeFix Mini FDA UDI
- Generic Name
- Implantable bone washer FDA UDI
- Device Name
- Spiked Washer 3.0mnm FDA UDI
- Model / Reference
- FX-HD-3100 FDA UDI
- Description
- Spiked Washer 3.0mnm FDA UDI
Identifiers
- Catalog Number
- FX-HD-3100 FDA UDI
- Primary DI / UDI-DI
- 00840124506893 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Implantable bone washer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Moist Heat or Steam Sterilization FDA UDI
Category: Implantable bone washer
FuzeFix Mini by Fusion Orthopedics, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Implantable bone washer.
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- FLAT WASHER — Biomet Orthopedics, Inc. · Class II
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- LEOS Cannulated Screw System — Tyber Medical · 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 |
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Manufacturer
- Manufacturer
- Fusion Orthopedics, Llc
Sources (1)
- FDA UDI 62c71eb9-98b3-4e7c-91dd-d131c4cd7ca3 34 fields · synced Jun 1, 2026