spineEOS 1.2
by Eos Imaging
spineEOS 1.2 is a Class II device made by Eos Imaging, listed in FDA GUDID since 10 Jul 2023 (UDI-DI 03663999000160), not in commercial distribution (GUDID) as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03663999000160 | Date10 Jul 2023 | StatusListed |
Official records
- AccessGUDID record 03663999000160
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- spineEOS
- Generic name
- Orthopaedic/craniofacial implantation planning software
- Model / reference
- 1.2
- Primary DI / UDI-DI
- 03663999000160
- FDA product code
- LLZ
- GMDN term
- Orthopaedic/craniofacial implantation planning software
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- Not in Commercial Distribution
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