# Lucenxia Prescience AG

- Location (FDA's records): Baar, CH
- FDA decisions: 9 (2013–2018): 9 510(k) clearances
- Product codes: KGO (9)
- 510(k) review time since 2016: median 141 days, against 153 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K173304: Finessis Intense Polyisoprene Surgical Glove (Apr 30, 2018)
- K173386: Finessis Zero Flexylon Powder Free Sterile White Surgical Glove Tested for use with Chemotherapy Drugs (Apr 9, 2018)
- K171987: Finessis Zero Flexylon Powder Free Sterile White Surgical Glove (Oct 20, 2017)
- K162852: Finessis Zero Chemo Flexylon Powder Free Sterile White Surgical Glove (Feb 8, 2017)
- K151605: Finessis Corium Flexylon Powder Free Sterile Green Surgical Gloves (Nov 16, 2015)
- K151607: Finessis Zero Flexylon Powder Free Sterile White Surgical Glove (Nov 16, 2015)
- K131751: Finessis Violet Element Polyisoprene Powderfree Sterile Surgical Gloves (Sep 25, 2013)
- K123629: Finessis Polyisoprene Powderfree Surgical Gloves (May 13, 2013)

Source page: https://510kreport.com/company/lucenxia-prescience