510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K884650Substantially Equivalent

Resubmitted Scanora

Orion Corp., 20101 Turku, FI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K884650 is the FDA 510(k) clearance record for RESUBMITTED SCANORA, a class II device, cleared for Orion Corp. on under FDA product code IZF (System, X-Ray, Tomographic). FDA records list 19 510(k) clearances for Orion Corp., from to . As of , FDA records show no recalls naming K884650.

Clearance record

Decision date
Received
(129 days to decision)
Product code
IZF System, X-Ray, Tomographic
Regulation
21 CFR 892.1740
Device class
Class II
Review panel
Radiology
Applicant
Orion Corp. P.O. Box 425, 20101 Turku, FI
Third party review
No

Clearances, product code IZF

Trailing 12 months
2 clearances under product code IZF 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 IZF, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260