# K253134: LAGIS Endoscopic Instruments- Scissors (EI-330S EI-330S-T EI-330MS EI-330MS-T)

- Pathway: 510(k) (Traditional)
- Applicant: Lagis Enterprise Co., Ltd.
- Decided: May 20, 2026 after 237 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: 2 generations back to K910831 (1991). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K984240: Endopath Endoscopic Instruments, Ethicon Endo-Surgery, Inc. (1999) Summary page 6.

## Indications for use
The LAGIS Endoscopic Instruments- Scissors have applications in minimally invasive procedures for cutting and cauterization of tissue.

Source page: https://510kreport.com/device/K253134
Methodology: https://510kreport.com/methodology