Identity
- Trade Name
- Inion Trinion™ FDA UDI
- Generic Name
- Meniscus screw FDA UDI
- Device Name
- 10 mm (x3) meniscus screw FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- 10 mm (x3) meniscus screw FDA UDI
Identifiers
- Catalog Number
- SET-3002 FDA UDI
- Primary DI / UDI-DI
- M224SET30029 FDA UDI
- 510(k) Number
- K031714 FDA UDI
- FDA Product Code
- HWC FDA UDI
- GMDN Term
- Meniscus screw FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Inion Trinion™ by Inion , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Inion , Ltd.
Sources (1)
- FDA UDI 7c95309d-0b0f-46c9-9079-62314fa95e9d 36 fields · synced May 31, 2026