510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K220355Substantially Equivalent

Astroglide Ultra Gentle Gel

Biofilm, Inc., Vista CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K220355 is the FDA 510(k) clearance record for Astroglide Ultra Gentle Gel, a class II device, cleared for Biofilm, Inc. on under FDA product code NUC (Lubricant, Personal). FDA's definition for product code NUC reads: "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...". FDA records list 17 510(k) clearances for Biofilm, Inc., from to . As of , FDA records show no recalls naming K220355.

Clearance record

Decision date
Received
(107 days to decision)
Product code
NUC Lubricant, Personal
Regulation
21 CFR 884.5300
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Biofilm, Inc. 3225 Executive Ridge, Vista CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NUC

Trailing 12 months
15 clearances under product code NUC in the twelve months to October 2026, December 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code NUC, trailing twelve months
MonthClearances
November 20250
December 20253
January 20260
February 20260
March 20261
April 20262
May 20261
June 20263
July 20262
August 20261
September 20262
October 20260