# K101782: Microstaar Msi Injector System Cartridge

- Pathway: 510(k) (Special)
- Applicant: Staar Japan
- Decided: Dec 22, 2010 after 180 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
Longest line of descent: 4 generations back to K914311 (1992). 10 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090161: Epiphany Injection System, Staar Surgical Co. (2009) Summary page 1.
- K073586: Microstaar Indigo Injector Foam Tip System, Staar Surgical Co. (2008) Summary page 1.
- K940593: Disposable Microstaar Injector, Staar Sugical (1994) Summary page 1.
- K980696: Foam Tip Injector, Staar Surgical Co. (1998) Summary page 1.

## Most influential descendants
- K172375: MicroSTAAR Injector System Cartridges (2017), 0 descendants of its own
- K152357: MicroSTAAR Injector System Cartridges (2015), 0 descendants of its own

## Indications for use
The MicroSTAAR™ MSI Injector System is a device intended to fold and insert STAAR™ Surgical Company Collamer phakic and aphakic one-piece and three-piece Collamer® intraocular lenses for surgical placement in the eye.

Source page: https://510kreport.com/device/K101782
Methodology: https://510kreport.com/methodology
