# K123310: Finesse 3RD Generation (Models Finesse+ and Finesseii+)

- Pathway: 510(k) (Traditional)
- Applicant: Utah Medical Products, Inc.
- Decided: Jan 23, 2013 after 90 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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 K941251 (1994). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K951032: Finess I (Dermatologic Application), Utah Medical Products, Inc. (1995) Summary page 1.
- K941251: Finesse Iec/601, Utah Medical Products, Inc. (1994) Summary page 2.

## Most influential descendants
- K133273: Liger Medical Esu-110 (2014), 0 descendants of its own

## Indications for use
The FINESSE+ and FINESSE II+ are intended to deliver high frequency electrical current for surgical procedures that can be performed with monopolar cutting and/or coagulation of tissue. One intended use of the FINESSE+ and FINESSE II+ systems is Loop Excision of the Transformation Zone (LETZ®).

Source page: https://510kreport.com/device/K123310
Methodology: https://510kreport.com/methodology