EndoSize 3.1
by Therenva Sas
EndoSize 3.1 is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Therenva Sas, listed in FDA GUDID since 19 Jul 2016 (UDI-DI 03760262480015), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03760262480015 | Date19 Jul 2016 | StatusListed |
Official records
- AccessGUDID record 03760262480015
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- EndoSize
- Generic name
- Radiology DICOM image processing application software
- Model / reference
- 3.1
- Primary DI / UDI-DI
- 03760262480015
- FDA product code
- LLZ
- GMDN term
- Radiology DICOM image processing application software
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- In Commercial Distribution
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