510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K093596Substantially Equivalent

Lumos, Model R 72B

Lumos, Inc., Naples FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K093596 is the FDA 510(k) clearance record for LUMOS, MODEL R 72B, a class II device, cleared for Lumos, Inc. on under FDA product code KPW (Device, Beam Limiting, X-Ray, Diagnostic). FDA records list one 510(k) clearance for Lumos, Inc. As of , FDA records show no recalls naming K093596.

Clearance record

Decision date
Received
(53 days to decision)
Product code
KPW Device, Beam Limiting, X-Ray, Diagnostic
Regulation
21 CFR 892.1610
Device class
Class II
Review panel
Radiology
Applicant
Lumos, Inc. 8726 Ferrara Ct., Naples FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KPW

Trailing 12 months

FDA records hold no clearances under product code KPW in the trailing twelve months.

FDA records show no clearances under product code KPW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260