Data / Medical devices / United States / Always More Marketing Inc
Always More Marketing Inc: FDA-registered device maker in Calabasas, CA, United States, 4 510(k) clearances
Always More Marketing Inc is registered with the FDA (registration 3009549313) in Calabasas, CA, United States. It lists 1 device type. The FDA files 4 510(k) clearances under its listings, the newest dated January 24, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009549313
- Address
- 24981 Palmilla Dr, Calabasas, CA, United States, 91302
- Owner or operator
- Always More Marketing Inc (10040371)
- Roles
- Specification developer
- First device listed
- April 5, 2012
- Registered through
- 2026
- Brand names listed
- Zyppah, Zyppah A, Zyppah Anti-Snoring Appliance, Zyppah V
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Anti-Snoring | LRK | 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 |
|---|---|---|---|---|---|---|
| January 24, 2019 | K182312 | Zyppah Anti-Snoring Device | LRK | Substantially Equivalent | Always More Marketing | accessdata.fda.gov |
| June 27, 2012 | K120372 | DR GREENBURGS HYBRID VACUUM | LRK | Substantially Equivalent | Always More Marketing, Inc. | accessdata.fda.gov |
| June 27, 2012 | K120371 | DR GREENBURGS HYBRID ACRYLIC | LRK | Substantially Equivalent | Always More Marketing, Inc. | accessdata.fda.gov |
| December 23, 2011 | K111680 | DR. GREENSBURG'S HYBRID | LRK | Substantially Equivalent | Always More Marketing, Inc. | accessdata.fda.gov |
Compare with other makers
Updated January 24, 2019. 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.