# K874106: Glandosane (Salivart) Synthetic Saliva

- Pathway: 510(k) (Traditional)
- Applicant: Fresenius USA, Inc.
- Decided: Apr 15, 1988 after 189 days
- Product code: LFD (Saliva, Artificial)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
28 later devices descend from it; 1 cites it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K991938: Caphosol Artificial Saliva (1999), 27 descendants of its own
- K030802: Caphosol (2003), 22 descendants of its own
- K024148: Salinum, Orclair (2003), 19 descendants of its own
- K051812: Tgo Spray (2005), 16 descendants of its own
- K061331: Oral Balance Liquid/ Gel (2006), 13 descendants of its own

Source page: https://510kreport.com/device/K874106
Methodology: https://510kreport.com/methodology