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

Personal Lubricant Ring

21 CFR 884.5300 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

QPD is the FDA product code for Personal Lubricant Ring, a class II device type, regulated under 21 CFR 884.5300. FDA's definition for this code reads: "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...". As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
QPD
Device name
Personal Lubricant Ring
FDA 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.
Regulation
21 CFR 884.5300
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code QPD

By decision year
1 clearance under product code QPD with a decision year between 2021 and 2021, 2021 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code QPD by decision year
YearClearances
20211

Applicants with the most clearances

Product code QPD
Applicants holding the most 510(k) clearances under product code QPD
ApplicantClearances
J3 Bioscience, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code