Identity
- Trade Name
- FX Shoulder Positioning System FDA UDI
- Generic Name
- Orthopaedic/craniofacial implantation planning software FDA UDI
- Device Name
- Planning software for total shoulder arthroplasty FDA UDI
- Model / Reference
- FXSPS001 FDA UDI
- Description
- Planning software for total shoulder arthroplasty FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760297030209 FDA UDI
- FDA Product Code
- LLZ FDA UDI
- GMDN Term
- Orthopaedic/craniofacial implantation planning software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.2050 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
Yes
FDA UDI
FX Shoulder Positioning System by Pixee Medical — 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
- Pixee Medical
Sources (1)
- FDA UDI 57a1ca4b-49a4-4380-8e00-bddab577f814 35 fields · synced Jun 8, 2026