# K180134: Ensizor Monopolar Endoscopic Scissors

- Pathway: 510(k) (Traditional)
- Applicant: Slater Endoscopy, LLC
- Decided: Jun 29, 2018 after 163 days
- Product code: KGE (Forceps, Biopsy, Electric)
- Device class: 2
- Regulation: 21 CFR 876.4300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K932648 (1993). 17 ancestors in all.
No later device cites it as a predicate yet.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150939: Ensizor Endoscopic Scissors, Slater Endoscopy, LLC (2015) Summary page 4.
- K090583: Endoscopic Monopolar Scissors, Models Ems-235, Ems-165, Apollo Endosurgery, Inc. (2009) Summary page 4.

## Indications for use
Ensizor® Monopolar Endoscopic Scissors are designed to cut and dissect tissue, cauterize tissue, cut sutures and cut non-metallic materials during all flexible endoscopic procedures..

Source page: https://510kreport.com/device/K180134
Methodology: https://510kreport.com/methodology