Data / Medical devices / United Kingdom / 1987 Media Limited
1987 Media Limited: FDA-registered device maker in Walton-On-Thames Surrey, United Kingdom, 1 510(k) clearance
1987 Media Limited is registered with the FDA (registration 3047906342) in Walton-On-Thames Surrey, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 10, 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
- 3047906342
- Address
- Alfa House Molesey Road, Walton-On-Thames Surrey, United Kingdom, KT12 3PD
- Owner or operator
- 1987 Media Limited (10096162)
- Roles
- Specification developer
- First device listed
- July 13, 2026
- Registered through
- 2026
- Brand names listed
- ClenchNoMore, TheSleepGuard
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mouthguard, Over-The-Counter | OBR | U | 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 |
|---|---|---|---|---|---|---|
| April 10, 2026 | K252485 | ClenchNoMore (CNM-1 (Mixed sizing)); ClenchNoMore (CNM-L (Large size)); ClenchNoMore (CNM-S (Small size)) | OBR | Substantially Equivalent | 1987 Media Limited | accessdata.fda.gov |
Compare with other makers
Updated April 10, 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.