# K011392: Micra Lens Injector, Micra Cartridge Lens, Micra Lens Loader

- Pathway: 510(k) (Traditional)
- Applicant: Micra Instruments
- Decided: Oct 22, 2001 after 168 days
- Product code: MSS (Folders And Injectors, Intraocular Lens (Iol))
- Device class: 1
- Regulation: 21 CFR 886.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K023737: Injector (2003), 1 descendant of its own
- K073010: Royale AE 9036 LSP Injector (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K011392
Methodology: https://510kreport.com/methodology