# K210693: Plexr Plus

- Pathway: 510(k) (Traditional)
- Applicant: Gmv S.R.L.
- Decided: Mar 22, 2022 after 379 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: 7 generations back to K933002 (1994). 15 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K192813: Plasma IQ, Neauvia North America, Inc. (2020) Summary page 4.

## Most influential descendants
- K242286: Superflow Prime Treatment System (ASP-1M) (2024), 0 descendants of its own

## Indications for use
Plexr Plus is used in the removal and destruction of skin lesions and coagulation of tissue.

Source page: https://510kreport.com/device/K210693
Methodology: https://510kreport.com/methodology