# K002845: Paflufocon C and E Daily Contact Lens

- Pathway: 510(k) (Traditional)
- Applicant: Paragon Vision Sciences
- Decided: Dec 8, 2000 after 87 days
- Product code: HQD (Lens, Contact (Other Material) - Daily)
- Device class: 2
- Regulation: 21 CFR 886.5916
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 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
- K051035: Synergeyes (Paflucon D Hem-Iberfilcon a) Hybrid Contact Lens (2005), 5 descendants of its own
- K052675: Synergeyes KC (Paflufocon D Hem-Iberfilcon a) Hybrid Contact Lens for Keratoconus (2005), 3 descendants of its own
- K060102: Synergeyes PS Hybrid Contact Lens (2006), 2 descendants of its own
- K142510: UltraHealth Hybrid Contact Lens for Keratoconus, UltraHealth Flat Cornea Hybrid Contact Lens (2014), 1 descendant of its own
- K083921: Synergeyes Sig (Petrafocon a Hem-Larafilcon a) Hybrid Contact Lens (2009), 1 descendant of its own

Source page: https://510kreport.com/device/K002845
Methodology: https://510kreport.com/methodology