# K252640: VereSee Optical Veres Needle and Endoscopic Camera

- Pathway: 510(k) (Traditional)
- Applicant: Freyja Healthcare, LLC
- Decided: Oct 20, 2025 after 60 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: 21 generations back to K930667 (1994). 109 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 111 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K243008: Arthrex NanoScope System, Arthrex, Inc. (2025) Summary page 5.
- K232464: VereSee Optical Veres Needle System, Freyja Healthcare, LLC (2024) Summary page 5.

## Most influential descendants
- K261139: VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103) (2026), 0 descendants of its own

## Indications for use
The VereSee Optical Veres Needle and Endoscopic Camera 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/K252640
Methodology: https://510kreport.com/methodology