Data / Medical devices / Germany / Lovehoney Group Germany GmbH
Lovehoney Group Germany GmbH: FDA-registered device maker in Berlin, Germany, 3 510(k) clearances
Lovehoney Group Germany GmbH is registered with the FDA (registration 3017022534) in Berlin, Germany. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated May 18, 2021. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3017022534
- Address
- Hermann Blankenstein Strass 5, Berlin, Germany, 10249
- Owner or operator
- Lovehoney Group US Trading Limited (10049880)
- Roles
- Exporter to the US
- First device listed
- March 1, 2021
- Registered through
- 2026
- Brand names listed
- ARCWAVE Lube 10ML, Arcwave Lube, We-Vibe Lube
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Exporter to the US | 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 18, 2021 | K202667 | Personal Lubricant Jelly | NUC | Substantially Equivalent | Nantong Health & Beyond Hygienic Products, Inc. | 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 |
| 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 18, 2021. 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.