# K914311: Chiroflex II Lens Microsert (TM)

- Pathway: 510(k) (Traditional)
- Applicant: Chiron Ophthalmics
- Decided: Jan 27, 1992 after 123 days
- Product code: HQL (Intraocular Lens)
- Device class: 3
- Regulation: 21 CFR 886.3600
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
18 later devices descend from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K970727: Mport Foldable Lens Placement System (1997), 17 descendants of its own
- K052651: C-Flex System Single Use Disposable Injector, Model R-Inj-02 (2006), 10 descendants of its own
- K062612: Rayner Single Use Soft Tipped Disposable Injector, Model R-Inj-04 (2006), 5 descendants of its own
- K091507: Rayner Small Incision Single Use Soft Tipped Injector, Model R-Inj-04/18 (2009), 3 descendants of its own
- K090161: Epiphany Injection System (2009), 3 descendants of its own

Source page: https://510kreport.com/device/K914311
Methodology: https://510kreport.com/methodology