Data / Medical devices / Luxembourg / pjur group Luxembourg S.A.
pjur group Luxembourg S.A.: FDA-registered device maker in Wasserbillig Luxembourg, Luxembourg, 7 510(k) clearances
pjur group Luxembourg S.A. is registered with the FDA (registration 3007957048) in Wasserbillig Luxembourg, Luxembourg. It lists 1 device type. The FDA files 7 510(k) clearances under its listings, the newest dated May 21, 2026. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007957048
- Address
- 87 Esplanade De La Moselle, Wasserbillig Luxembourg, Luxembourg, 6637
- Owner or operator
- pjur Group Luxembourg SA (10036525)
- Roles
- Specification developer
- First device listed
- May 13, 2011
- Registered through
- 2026
- Brand names listed
- pjur AQUA, pjur AQUA Aloe Vera, pjur AQUA Naked, pjur AQUA Natural, pjur BACK DOOR Moisturizing, pjur BACK DOOR Relaxing, pjur BASIC Silicone, pjur BASIC Water-based and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 21, 2026 | K260068 | pjur NATURE Touch, 100 ml | NUC | Substantially Equivalent | Pjur Group Luxembourg S.A. | accessdata.fda.gov |
| February 19, 2021 | K200527 | pjur WOMAN Aloe, pjur analyse me! water-based, pjur BACK DOOR water-based, pjur med Moisturising glide,pjur med NATURAL glide, We-Vibe Lube made by pjur | NUC | Substantially Equivalent | Pjur Group Luxembourg S.A. | accessdata.fda.gov |
| December 17, 2020 | K200730 | pjur WOMAN Nude pjur med SENSITIVE glide | NUC | Substantially Equivalent | Pjur Group Luxembourg S.A. | accessdata.fda.gov |
| April 6, 2015 | K141913 | PJUR SILICONE BASED LUBRICANT: PJUR BACKDOOR ANAL GLIDE AND ANALYSE ME! | NUC | Substantially Equivalent | Pjur Group Luxembourg S.A. | accessdata.fda.gov |
| July 24, 2014 | K133336 | PJUR(R) SILICONEGEL, PJUR(R) BASIC PERSONAL GLIDE, PJUR(R) LIGHT, PJUR(R) MED PREMIUM GLIDE | NUC | Substantially Equivalent | Pjur Group Luxembourg S.A. | accessdata.fda.gov |
| July 18, 2014 | K133233 | PJUR ORIGINAL, PJUR WOMAN, PJUR MAN EXTREME GLIDE | NUC | Substantially Equivalent | Pjur Group Luxembourg S.A. | accessdata.fda.gov |
| April 5, 2001 | K010199 | PJUR EROS WATER FORMULATION | NUC | Substantially Equivalent | L.C.C. Pjur Group Germany | accessdata.fda.gov |
Compare with other makers
Updated May 21, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.