Identity
- Trade Name
- Kyocera Medical Technologies, Inc. FDA UDI
- Generic Name
- Orthopaedic bone screw (non-sliding) FDA UDI
- Device Name
- 4.0mm Cannulated Screw, Full Thread, L 22mm FDA UDI
- Model / Reference
- T 700 FDA UDI
- Description
- 4.0mm Cannulated Screw, Full Thread, L 22mm FDA UDI
Identifiers
- Catalog Number
- 1701-405-022 FDA UDI
- Primary DI / UDI-DI
- 00841523113057 FDA UDI
- 510(k) Number
- K092082 FDA UDI
- FDA Product Code
- HWC FDA UDIHTN FDA UDI
- GMDN Term
- Orthopaedic bone screw (non-sliding) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3030 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Kyocera Medical Technologies, Inc. by Kyocera Medical Technologies, Inc. — 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
- Kyocera Medical Technologies, Inc.
Sources (1)
- FDA UDI 0764af6f-8984-437f-a596-2a688d426995 36 fields · synced Jun 8, 2026