Identity
- Trade Name
- EXULT Knee Replacement System FDA UDI
- Generic Name
- Knee tibia prosthesis trial, reusable FDA UDI
- Device Name
- Tibial Insert Trial UCR #06 T16 FDA UDI
- Model / Reference
- KA.IUC.R616 FDA UDI
- Description
- Tibial Insert Trial UCR #06 T16 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809945894055 FDA UDI
- 510(k) Number
- K250889 FDA UDI
- FDA Product Code
- JWH FDA UDI
- GMDN Term
- Knee tibia prosthesis trial, reusable 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
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Knee tibia prosthesis trial, reusable
EXULT Knee Replacement System by Corentec Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K250889 also covers:
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement System — Corentec Co., Ltd
- EXULT Knee Replacement 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 f1908d2c-e2cd-4a7b-a235-6922e6060b28 35 fields · synced May 31, 2026