510(k) · Cleared
ClearedAstroglide X Silicone Personal Lubricant
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Biofilm, Inc. · NUC Lubricant, Personal
Cleared on Apr 28, 2021 as substantially equivalent to K141913 (Pjur Group Luxembourg S.A., 2015) after an 89-day review. Its family tree reaches back 4 generations to 2006.
- Decided
- Apr 28, 2021
- Review
- 89 days
- Class
- Class II
- Product code
- NUC
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 4 generations to K062796 (2006). No later device cites it as a predicate yet.
- Root · 4 generations backK062796 K-Y Brand IntriguePersonal Products Co. · 2006
- 3 generations backK110690 One Personal Lubricant (Silicone)One · 2012
- 2 generations backK130012 Wet Platinum Personal LubricantTrigg Laboratories, Inc. · 2013
- 1 generation backK141913 Pjur Silicone Based Lubricant: Pjur Backdoor Anal Glide and Analyse…Pjur Group Luxembourg S.A. · 2015
- This deviceK210242 Astroglide X Silicone Personal LubricantBiofilm, Inc. · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K062796 | K-Y Brand Intrigue | Personal Products Co. | 2006 | — |
| −3 | K110690 | One Personal Lubricant (Silicone) | One | 2012 | — |
| −2 | K130012 | Wet Platinum Personal Lubricant | Trigg Laboratories, Inc. | 2013 | — |
| −1 | K141913 | Pjur Silicone Based Lubricant: Pjur Backdoor Anal Glide and Analyse ME! | Pjur Group Luxembourg S.A. | 2015 | — |
| 0 (this device) | K210242 | Astroglide X Silicone Personal Lubricant | Biofilm, Inc. | 2021 | — |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in NUC? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new NUC device
- #1 K211998 Desnuda Reflectscore 18.6 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K141913 | Pjur Silicone Based Lubricant: Pjur Backdoor Anal Glide and Analyse ME!Summary page 4…Predicate Device 510(k) Number pjur@ Backdoor Anal Glide and pjur@ K141913 Analyse Me! This predicate device has not been subject to a device-related recall. iv. Description of De… | 2015 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 15 years and passes through 5 companies; a new generation was cleared every 5.3 years on median.
- None of the 4 ancestors has a recall.
- 1 other device also cites its predicate K141913.
How does its category compare?
All NUC devicesNUC Lubricant, Personal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · NUC
11in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · NUC
221in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NUC
3in 2013
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NUC
13in 2025
MAUDE reports naming product code NUC, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 5 | 150 | 0 | 0 |
| 2008 | 7 | 271 | 1 | 6 |
| 2009 | 2 | — | 1 | 13 |
| 2010 | 4 | 124 | 0 | 2 |
| 2011 | 2 | — | 0 | 3 |
| 2012 | 6 | 269 | 0 | 6 |
| 2013 | 11 | 205 | 3 | 5 |
| 2014 | 11 | 264 | 0 | 14 |
| 2015 | 21 | 251 | 0 | 8 |
| 2016 | 14 | 181 | 0 | 14 |
| 2017 | 14 | 175 | 0 | 19 |
| 2018 | 15 | 114 | 0 | 6 |
| 2019 | 13 | 150 | 0 | 8 |
| 2020 | 19 | 180 | 0 | 2 |
| 2021 | 20 | 143 | 0 | 7 |
| 2022 | 14 | 112 | 0 | 7 |
| 2023 | 13 | 159 | 0 | 15 |
| 2024 | 6 | 178 | 0 | 13 |
| 2025 | 11 | 221 | 0 | 13 |
| 2026 | 12 | 104 | 0 | — |
What is it indicated for?
Astroglide@ X Silicone Personal Lubricant is a personal lubricant for penile, vaginal, and/or anal 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 is compatible with natural rubber latex condoms. This product is not compatible with polyisoprene and polyurethane condoms.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K210242 · printed Nov 6, 2026
Cite this page
510(k) Report. “K210242: Astroglide X Silicone Personal Lubricant.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K210242
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026