# Always More Marketing, Inc.

- Location (FDA's records): Las Vegas, NV
- FDA decisions: 4 (2011–2019): 4 510(k) clearances
- Names in FDA's records: Always More Marketing, Inc. (3); Always More Marketing (1)
- Product codes: LRK (4)
- Predicates its devices cite: 18 (3 its own); citations of its devices by later devices: 6 (3 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Tomed Dr. Toussaint GmbH: 3 (https://510kreport.com/company/tomed-dr-toussaint)
- Bryan Keropian Dds: 3 (https://510kreport.com/company/bryan-keropian-dds)
- Glidewell Laboratories: 3 (https://510kreport.com/company/glidewell-laboratories)
- Frantz Design, Inc.: 3 (https://510kreport.com/company/frantz-design)
- Dennis R. Bailey, Dds: 1 (https://510kreport.com/company/dennis-r-bailey-dds)
- The Snore Reliever Company, LLC: 1 (https://510kreport.com/company/snore-reliever)
- Respire Medical: 1 (https://510kreport.com/company/respire-medical)

## Firms that cite its devices most
- Myofunctional Research Corp. Pty., Ltd.: 2 (https://510kreport.com/company/myofunctional-research)
- Dasoft Partners: 1 (https://510kreport.com/company/dasoft-partners)

## Its most-cited devices
- K111680: DR. Greensburg's Hybrid (2011), cited by 4
- K182312: Zyppah Anti-Snoring Device (2019), cited by 2

## Recent decisions
- K182312: Zyppah Anti-Snoring Device (Jan 24, 2019)
- K120372: DR Greenburgs Hybrid Vacuum (Jun 27, 2012)
- K120371: DR Greenburgs Hybrid Acrylic (Jun 27, 2012)
- K111680: DR. Greensburg's Hybrid (Dec 23, 2011)

Source page: https://510kreport.com/company/always-more-marketing