Identity
- Trade Name
- LOSPA Total Knee System FDA UDI
- Generic Name
- Uncoated knee tibia/insert prosthesis FDA UDI
- Device Name
- LOSPA Tibial Insert (CR) FDA UDI
- Model / Reference
- 01.10.1BG FDA UDI
- Description
- LOSPA Tibial Insert (CR) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08806373821929 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Uncoated knee tibia/insert prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3560 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
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
No
FDA UDI
Category: Uncoated knee tibia/insert prosthesis
LOSPA Total Knee System by Corentec Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Uncoated knee tibia/insert prosthesis.
- Arthrex® — Arthrex, Inc. · Class II
- Vanguard Complete Knee System — Biomet Orthopedics, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Vanguard Knee System — Biomet Orthopedics, Inc. · Class II
- Vanguard® Complete Knee System — Biomet Orthopedics, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
- Arthrex® — Arthrex, Inc. · Class II
Cleared under the same submission
K110404 also covers:
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
K130673 also covers:
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Knee System — Corentec Co., Ltd
- LOSPA Total Knee System — Corentec Co., Ltd
- LOSPA Total Knee System — Corentec Co., Ltd
- LOSPA Total Knee System — Corentec Co., Ltd
- LOSPA Total Knee System — Corentec Co., Ltd
- LOSPA Total Knee System — Corentec Co., Ltd
- LOSPA Total Knee System — Corentec Co., Ltd
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
- Corentec Co., Ltd
Sources (1)
- FDA UDI efe90376-5139-4779-b86a-8ff785a4558d 35 fields · synced May 31, 2026