DeviceClearance

Product code QPD— Obstetrics/Gynecology

VR101 Lubricating Intravaginal Ring

Classification name
Personal Lubricant Ring
Device class
Class 2
Regulation
21 CFR 884.5300
Advisory panel
Obstetrics/Gynecology
Total cleared
1
First cleared
Most recent

FDA classification definition

“This device is a personal lubricant, for 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, polyurethane, and/or internal condoms.”

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

Market context for product code QPD

FDA has cleared 1 device under product code QPD, all in 2021, filed by 1 applicant company. 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.

Top applicants under product code QPD

Recent clearances under product code QPD

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