# P170035: Bausch + Lomb Ultra (samfilcon A) Contact Lenses

- Pathway: PMA
- Applicant: Bausch and Lomb, Inc.,
- Decided: Apr 30, 2018 after 180 days
- Product code: LPM (Lenses, Soft Contact, Extended Wear)
- Device class: 3
- Regulation: 21 CFR 886.5925
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P170035
Methodology: https://510kreport.com/methodology