Identity
- Trade Name
- DynaForce FDA UDI
- Generic Name
- Instrument tray, reusable FDA UDI
- Device Name
- DynaForce Staple Instruments Tray FDA UDI
- Model / Reference
- DynaForce Staple Instruments Tray FDA UDI
- Description
- DynaForce Staple Instruments Tray FDA UDI
Identifiers
- Catalog Number
- 245070PKG FDA UDI
- Primary DI / UDI-DI
- 00810112597615 FDA UDI
- 510(k) Number
- K202268 FDA UDI
- FDA Product Code
- KCT FDA UDI
- GMDN Term
- Instrument tray, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6850 FDA UDI
- Commercial Distribution
- Not 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
DynaForce by Crossroads Extremity Systems Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K202268 also covers:
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
- Crossroads Extremity Systems Llc
Sources (1)
- FDA UDI d89e0c46-c0d2-40d6-b490-6451d6259cce 36 fields · synced Jun 1, 2026