510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K150828Substantially Equivalent

O-RING Condom

O-Ring Products, LLC, Raleigh NC / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K150828 is the FDA 510(k) clearance record for O-RING Condom, a class II device, cleared for O-Ring Products, LLC on under FDA product code HIS (Condom). FDA records list one 510(k) clearance for O-Ring Products, LLC. As of , FDA records show no recalls naming K150828.

Clearance record

Decision date
Received
(263 days to decision)
Product code
HIS Condom
Regulation
21 CFR 884.5300
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
O-Ring Products, LLC 4012 Grand Manor Ct. #208, Raleigh NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HIS

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