510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962290Substantially Equivalent

Deroyal Industries, Inc. Neonatal Eye Cover

Debusk Technology Corp., Powell TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962290 is the FDA 510(k) clearance record for DEROYAL INDUSTRIES, INC. NEONATAL EYE COVER, a class I device, cleared for Debusk Technology Corp. on under FDA product code FOK (Pad, Neonatal Eye). FDA records list 4 510(k) clearances for Debusk Technology Corp., from to . As of , FDA records show no recalls naming K962290.

Clearance record

Decision date
Received
(19 days to decision)
Product code
FOK Pad, Neonatal Eye
Regulation
21 CFR 880.5270
Device class
Class I
Review panel
General Hospital
Applicant
Debusk Technology Corp. 200 Debusk Ln., Powell TN
510(k) summary
Summary
Third party review
No

Clearances, product code FOK

Trailing 12 months

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

FDA records show no clearances under product code FOK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FOK, 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