Identity
- Trade Name
- Kinos Instrumentation FDA UDI
- Generic Name
- Joint prosthesis implantation kit, reusable FDA UDI
- Device Name
- Range Surface Talar Prep Guide, Size 3, Right FDA UDI
- Model / Reference
- 5871-2723 FDA UDI
- Description
- Range Surface Talar Prep Guide, Size 3, Right FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840097515427 FDA UDI
- 510(k) Number
- K240591 FDA UDI
- FDA Product Code
- HSN FDA UDI
- GMDN Term
- Joint prosthesis implantation kit, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3110 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Joint prosthesis implantation kit, reusable
Kinos Instrumentation by Restor3D — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Joint prosthesis implantation kit, reusable.
- Initia Total Hip System — Kyocera Corporation · Class II
- PROPHECY — MicroPort Orthopedics Inc. · Class II
- Cadence Total Ankle System — Smith & Nephew, Inc. · Class I
- IMPLANT PARTNERS™ — MicroPort Orthopedics Inc. · Class I
- Evolution — MicroPort Orthopedics Inc. · Class II
- GUARDIAN® — MicroPort Orthopedics Inc. · Class I
- ADVANCE® — MicroPort Orthopedics Inc. · Class I
- PROPHECY — MicroPort Orthopedics Inc. · Class II
Cleared under the same submission
K240591 also covers:
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
- Kinos Instrumentation — Restor3D
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Restor3D
Sources (1)
- FDA UDI a21dd333-65b7-46eb-a281-909764a38f1a 34 fields · synced May 30, 2026