DeviceClearance

Product code NUC— Obstetrics/Gynecology

ALOE CADABRA LUBRICANT, ALOE CADABRA FLAVORED/SCENTED LUBRICANTS

Classification name
Lubricant, Personal
Device class
Class 2
Regulation
21 CFR 884.5300
Advisory panel
Obstetrics/Gynecology
Total cleared
248
First cleared
Most recent

FDA classification definition

“This device is a personal lubricant, for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity, and supplement the body's natural lubrication. This product may or may not be compatible with natural rubber latex, polyisoprene, and/or polyurethane condoms.”

— U.S. Food and Drug Administration, device classification record for product code NUC under 21 CFR 884.5300, via openFDA

Market context for product code NUC

FDA has cleared 248 devices under product code NUC between 2000 and 2026, filed by 138 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code NUC

Adverse events under product code NUC

product code NUC
Other
8
Total
8

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code NUC

1–100 of 248

Data sourced from openFDA. This site is unofficial and independent of the FDA.