# K261139: VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)

- Pathway: 510(k) (Traditional)
- Applicant: Freyja Healthcare, LLC
- Decided: Aug 13, 2026 after 128 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 22 generations back to K930667 (1994). 110 ancestors in all.
No later device cites it as a predicate yet.
0 of 111 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K252640: VereSee Optical Veres Needle and Endoscopic Camera, Freyja Healthcare, LLC (2025) Summary page 5.

## Indications for use
VereSee is intended for: • Percutaneous insertion into the peritoneal cavity for the purpose of insufflation with carbon dioxide to establish pneumoperitoneum prior to the placement of trocars during laparoscopic surgery • Use as an endoscopic video camera to provide visible light imaging in a variety of endoscopic and laparoscopic diagnostic and surgical procedures

Source page: https://510kreport.com/device/K261139
Methodology: https://510kreport.com/methodology