510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K984178Substantially Equivalent

Pronosco X-Posure System

Torsana Osteoporosis Diagnostics A/S, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K984178 is the FDA 510(k) clearance record for PRONOSCO X-POSURE SYSTEM, a class II device, cleared for Torsana Osteoporosis Diagnostics A/S on under FDA product code KGI (Densitometer, Bone). FDA records list one 510(k) clearance for Torsana Osteoporosis Diagnostics A/S. As of , FDA records show no recalls naming K984178.

Clearance record

Decision date
Received
(90 days to decision)
Product code
KGI Densitometer, Bone
Regulation
21 CFR 892.1170
Device class
Class II
Review panel
Radiology
Applicant
Torsana Osteoporosis Diagnostics A/S 555 13th St., NW, Washington DC
510(k) summary
Summary
Third party review
No

Clearances, product code KGI

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