Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K211108Substantially Equivalent

Prudent 1717, Prudent 1417, Prudent 1212

PixxGen Corporation, Anyang-Si, KR / Traditional, Substantially Equivalent

K211108 is the FDA 510(k) clearance record for Prudent 1717, Prudent 1417, Prudent 1212, a class II device, cleared for Pixxgen Corporation on under FDA product code MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager)). FDA records list 4 510(k) clearances for Pixxgen Corporation, from to . As of , FDA records show no recalls naming K211108.

Clearance record

Decision date
Received
(51 days to decision)
Product code
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)
Regulation
21 CFR 892.1680
Device class
Class II
Review panel
Radiology
Applicant
Pixxgen Corporation 5f, Smart Bay, 123, Beolmal-Ro, Dongan-Gu,, Anyang-Si, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MQB

Trailing 12 months
3 clearances under product code MQB in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code MQB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20262
July 20261
August 20260
September 20260
October 20260