Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K203116Substantially Equivalent

SensorX

Durr Dental SE, Bietigheim-Bissingen, DE / Traditional, Substantially Equivalent

K203116 is the FDA 510(k) clearance record for SensorX, a class II device, cleared for Durr Dental SE on under FDA product code MUH (System, X-Ray, Extraoral Source, Digital). FDA records list 11 510(k) clearances for Durr Dental SE, from to . As of , FDA records show no recalls naming K203116.

Clearance record

Decision date
Received
(154 days to decision)
Product code
MUH System, X-Ray, Extraoral Source, Digital
Regulation
21 CFR 872.1800
Device class
Class II
Review panel
Dental
Applicant
Durr Dental SE Hopfigheimer St. 17, Bietigheim-Bissingen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MUH

Trailing 12 months
2 clearances under product code MUH in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MUH, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260