# Therenva Sas

- Location (FDA's records): Rennes, FR
- FDA decisions: 5 (2014–2022): 5 510(k) clearances
- Product codes: OWB (3), LLZ (2)
- 510(k) review time since 2016: median 78 days, against 83 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 6 (4 its own); citations of its devices by later devices: 7 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Cydar, Ltd.: 1 (https://510kreport.com/company/cydar)
- Pie Medical Imaging BV: 1 (https://510kreport.com/company/pie-medical-imaging)

## Firms that cite its devices most
- Endo Vantage, LLC: 1 (https://510kreport.com/company/endo-vantage)
- Brainlab AG: 1 (https://510kreport.com/company/brainlab)
- Cydar, Ltd.: 1 (https://510kreport.com/company/cydar)

## Its most-cited devices
- K141475: Endosize (2014), cited by 2
- K160376: EndoSize (2016), cited by 2
- K212383: EndoNaut (2021), cited by 1
- K222070: EndoNaut (2022), cited by 1
- K171829: EndoNaut (2017), cited by 1

## Recent decisions
- K222070: EndoNaut (Oct 25, 2022)
- K212383: EndoNaut (Aug 31, 2021)
- K171829: EndoNaut (Sep 21, 2017)
- K160376: EndoSize (Apr 12, 2016)
- K141475: Endosize (Jul 31, 2014)

Source page: https://510kreport.com/company/therenva