Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: LTZ FDA class 2

Condom With Nonoxynol-9

Obstetrics/Gynecology

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Condom with Nonoxynol-9 (product code LTZ) is a male barrier contraceptive device made of latex or similar material coated with nonoxynol-9, a spermicidal agent intended to provide both contraceptive protection and additional prophylactic activity against sexually transmitted infections. Regulated under 21 CFR 884.5310 and classified as a Class 2 device, it requires a 510(k) premarket notification and is eligible for third-party review under the Obstetrics/Gynecology panel. It is not an implant and is not life-sustaining.

510(k) Clearances

22 matches
K Number
Device Name
CAUTION CONDOMS
DOUBLE SPRINGERS NONOXNOL 9 CONDOM
SPERMICIDAL LUBRICATED MALE LATEX CONDOM
CONTROL MALE CONDOMS OF NATURAL RUBBER LATEX
'ONE TOUCH' LATEX CONDOM WITH NONOXYNOL-9
SPERMICIDAL LUBRICATED MALE LATEX CONDOM
INVIGRA PLUS (WITH SPERMICIDAL LUBRICANT)
HARDCOVER CONDOMS MALE LATEX CONDOMS, (WITH SPERMICIDE)
MULTIPLE-BRAND MALE LATEX CONDOM (LUBRICATED WITH NONOXYNOL-9)
MAXIMA, TRUSTEX, RIA AND PREMIUM EL LES CONDOMS
ROYALE OF LATEX CONDOMS - SPERMICIDAL LUBRICANT - COLORED OR ASSORTED COLORS
LATEX CONDOMS COLOUR WITH SPERMICIDAL LUBRICANT
LATEX CONDOMS (NATURAL COLOUR)
ROYALE BRAND LATEX CONDOMS-SPERMICIDAL LUBRICANT - COLORED OR ASSORTED COLORS
INNERWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9
EXTRAWEAR, GENTLEMEN'S CHOICE W/NONOXYNOL-9
INNERWEAR/EXTRAWEAR/JIMMY-O RAINCOAT/ZEUS/GENTLEMEN'S CHOICE/JASMINE/DRINK/NAUGHTY
OLYMPUS,JASMINE,JIMMY-O RAINCOAT,DRINK,ARES,APHRODITE,ZEUS,APOLLO,SELFCARE,CAREPLUS,TITAN
LONDON ROYAL CONSUMER PRODUCTS LATEX CONDOMS
DUREX, RAMSES, SHEIK
SPERMICIDAL LUBRICATED CONDOM
MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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