Identity
- Trade Name
- STAR™ FDA UDI
- Generic Name
- Ankle prosthesis bearing FDA UDI
- Device Name
- Sliding Core, UHMPWE, 9mm FDA UDI
- Model / Reference
- 400-143F FDA UDI
- Description
- Sliding Core, UHMPWE, 9mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00886385026954 FDA UDI
- FDA Product Code
- NTG FDA UDI
- GMDN Term
- Ankle prosthesis bearing FDA UDI
Classification
- Device Class
- Class III 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
Dimensions & Sizes
- Size
- Height — 9 Millimeter FDA UDI
Category: Ankle prosthesis bearing
Star™ by Stryker Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ankle prosthesis bearing.
- Kinos Total Ankle Replacement — Restor3D · Class II
- Hintermann Series H2 — Vilex, Inc. · Class II
- Kinos Total Ankle Replacement — Restor3D · Class II
- Hintermann Series H3 — Dt Medtech, LLC · Class III
- Hintermann Series H2 — Dt Medtech, LLC · Class II
- Hintermann Series H2 — Dt Medtech, LLC · Class II
- Kinos Total Ankle Replacement — Restor3D · Class II
- Hintermann Series H2 — Vilex, Inc. · 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 III | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 2e7ba6a0-dee1-4c04-890a-a2cc675a4f30 36 fields · synced Jun 6, 2026