Identity
- Trade Name
- FUSEFORCE FDA UDI
- Generic Name
- Orthopaedic fixation plate, non-bioabsorbable, non-sterile FDA UDI
- Model / Reference
- FFS-2522 FDA UDI
Identifiers
- Catalog Number
- FFS-2522 FDA UDI
- Primary DI / UDI-DI
- 00840420168009 FDA UDI
- FDA Product Code
- JDR FDA UDI
- GMDN Term
- Orthopaedic fixation plate, non-bioabsorbable, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
No
Contains Latex
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
Yes
Dimensions & Sizes
- Size
- Length — 22 Millimeter FDA UDI
Category: Orthopaedic fixation plate, non-bioabsorbable, non-sterile
Introducing the FUSEFORCE, a non-sterile implantable sheet used for orthopedic fixation plate applications. This device is designed to bridge and stabilize fractured long bone fragments, shielding the site from stress as the bone heals. The FUSEFORCE has been certified in commercial distribution and has undergone thorough testing for its sterilization, expiration date, and labeling compliance.
Similar devices
Also classified as Orthopaedic fixation plate, non-bioabsorbable, non-sterile.
- Proximal Humeral Locking Plate Ⅱ, Combi-holes — Double Medical Technology Inc. · Class II
- Summa Orthopaedics Wrist System Bone Plate — Jeil Medical Corporation · Class II
- Summa Orthopaedics Foot System Bone Plate — Jeil Medical Corporation · Class II
- SAMPEDRO — Industrias Medicas Sampedro S.A.S · Class II
- TUBULAR PLATE — Biomet Orthopedics, Inc. · Class II
- APTUS — Medartis Inc. · Class II
- VERUM Foot System Bone Plate — Jeil Medical Corporation · Class II
- 3.5 LC TI polyaxial locking plate, str., 20 h., 242mm — mahe medical gmbh · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
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
- Wright Medical Technology, Inc.
Sources (1)
- FDA UDI 367a0c46-1eea-4a4c-b723-8674c43c85fa 35 fields · synced Oct 6, 2026