510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140703Substantially Equivalent

Opa 30 Solution

Ciden Technologies, LLC, Orange CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140703 is the FDA 510(k) clearance record for OPA 30 SOLUTION, a class II device, cleared for Ciden Technologies, LLC on under FDA product code MED (Sterilant, Medical Devices). FDA records list 2 510(k) clearances for Ciden Technologies, LLC, from to . As of , FDA records show no recalls naming K140703.

Clearance record

Decision date
Received
(152 days to decision)
Product code
MED Sterilant, Medical Devices
Regulation
21 CFR 880.6885
Device class
Class II
Review panel
General Hospital
Applicant
Ciden Technologies, LLC 1717 W. Collins Ave., Orange CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code MED

Trailing 12 months
1 clearance under product code MED 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 MED, 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 20260
October 20260