XVbeam2000— 510(k) K233914

Name: FDA 510(k) clearance K233914
Creator: U.S. Food and Drug Administration
Published: 2024-02-08

Substantially Equivalent

Shenzhen Xpectvision Technology Co., Ltd.

FDA 510(k) clearance K233914 for XVbeam2000, Substantially Equivalent on 2024-02-08. Applicant: Shenzhen Xpectvision Technology Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Xpectvision Technology Co., Ltd.
Product code: Code EHD
Device class: Class 2
Regulation: 21 CFR 872.1800
Advisory panel: Dental
Date received: 2023-12-12
Decision date: 2024-02-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: No.44 Xiangrui 3rd Road, Nanshan Distric, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code EHD

view all

K260367 — Portable Dental X-ray System Model PDX nova2026-05-27
K253864 — NOMAD Pro 32026-03-20
K252110 — Dental X-RAY Unit (AJX200)2026-03-12
K254018 — Portable Dental X-ray Device (GT-1)2026-02-19
K252909 — Diagnostic X-Ray Equipment Model POCT222026-02-03

More clearances from Shenzhen Xpectvision Technology Co., Ltd.

view all

K220277 — Digital Intraoral X-ray Sensor2022-02-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.