Orthopantomograph OP 3D LX— 510(k) K230505

Substantially Equivalent

Palodex Group OY

FDA 510(k) clearance K230505 for Orthopantomograph OP 3D LX, Substantially Equivalent on 2023-06-09. Applicant: Palodex Group OY. Device class: 2.

Clearance details

Applicant: Palodex Group OY
Product code: Code OAS
Device class: Class 2
Regulation: 21 CFR 892.1750
Advisory panel: Radiology
Date received: 2023-02-24
Decision date: 2023-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tuusula, FI

Download summary PDF View on FDA.gov ↗

Recent devices under product code OAS

K261748 — Dental Cone-beam Computed Tomography (mDX-15P Series)2026-07-23
K250839 — Dental X-ray System2026-06-11
K260662 — Dental Cone Beam Computed Tomography System2026-06-04
K253935 — medXion NEXUS2026-05-15
K260462 — RCT8002026-04-09

More clearances from Palodex Group OY

K241249 — Orthopantomograph OP 3D LX (PAN 3D); Orthopantomograph OP 3D LX (PAN CEPH 3D)2024-09-12
K180947 — Orthopantomograph OP 3D2018-06-07
K173646 — FS Ergo2017-12-19
K163423 — Orthopantomograph OP3002017-08-31
K162799 — Cliniview2017-04-25

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