# K180350: Dornier Medilas H Solvo 35 Laser

- Pathway: 510(k) (Special)
- Applicant: Dornier Medtech America
- Decided: Mar 7, 2018 after 27 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K936109 (1994). 33 ancestors in all.
No later device cites it as a predicate yet.
0 of 34 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122159: Dornier Medilas H30 Solvo, Dornier Medtech America, Inc. (2013) Summary page 4.

## Indications for use
The Solvo 35W is intended to be used for cutting, vaporization, ablation, and coagulation of soft tissue in conjunction with endoscopic equipment (including laparoscopes, hysteroscopes, bronchoscopes, gastroscopes, cystoscopes, and colonoscopes), or for open surgery for contact or non-contact surgery with or without a handpiece for use in incision/excision, vaporization, ablation and coagulation of soft tissue. The Solvo 35W is indicated for use in medicine and surgery, in the following medical specialties: . Arthroscopy . Urology . Lithotripsy . Pulmonology . Gastroenterology . Gynecology . ENT . General Surgery

Source page: https://510kreport.com/device/K180350
Methodology: https://510kreport.com/methodology