# K011773: Dornier Lithotripter 140(Doli 140)

- Pathway: 510(k) (Special)
- Applicant: Dornier
- Decided: Jun 22, 2001 after 15 days
- Product code: LNS (Lithotriptor, Extracorporeal Shock-Wave, Urological)
- Device class: 2
- Regulation: 21 CFR 876.5990
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to P840008 (1984). 2 ancestors in all.
7 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002929: Dornier Compact Alpha Lithotripter, Dornier Medtech America, Inc. (2001) Summary page 1.
- P840008: Dornier Lithotripter Compact Transportable (DLCT), Dornier Medtech America, Inc. (1984) Summary page 1.

## Most influential descendants
- K121656: Gemini Lithotripter (2012), 6 descendants of its own
- K133434: Genesis II (2014), 2 descendants of its own
- K151485: Genesis (2015), 1 descendant of its own
- K132672: Extra Corporeal Shockwave Lithotripter (2013), 1 descendant of its own
- K220871: Nautilus (2022), 0 descendants of its own

## Indications for use
The Dornier Lithotripter 140 (“Doli 140”) is indicated for fragmentation of urinary tract stones, i.e. renal calyceal stones, renal pelvic stones, and upper ureteral stones.

Source page: https://510kreport.com/device/K011773
Methodology: https://510kreport.com/methodology