Durex Play Soft & Sensual Lubricant
K071626 is the FDA 510(k) clearance record for DUREX PLAY SOFT & SENSUAL LUBRICANT, a class II device, cleared for Ssl Americas 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 16 510(k) clearances for Ssl Americas, from to . As of , FDA records show no recalls naming K071626.
Clearance record
- Decision date
- Received
- (292 days to decision)
- Product code
- NUC Lubricant, Personal
- Regulation
- 21 CFR 884.5300
- Device class
- Class II
- Review panel
- Obstetrics/Gynecology
- Applicant
- Ssl Americas 3583 Engineering Dr. Suite 200, Norcross GA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code NUC
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 3 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 1 |
| April 2026 | 2 |
| May 2026 | 1 |
| June 2026 | 3 |
| July 2026 | 2 |
| August 2026 | 1 |
| September 2026 | 2 |
| October 2026 | 0 |
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What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
