Always More Marketing Inc
Also registered as Always More Marketing
United Statesfrom the FDA registration address FDA establishment FEI 3009549313
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dr Greenburgs Hybrid Acrylic Ref K120371
Regimes: 510(k) Registry: 510(k)Zyppah Anti-Snoring Device Ref K182312
Regimes: 510(k) Registry: 510(k)Dr Greenburgs Hybrid Vacuum Ref K120372
Regimes: 510(k) Registry: 510(k)Dr. Greensburg's Hybrid Ref K111680
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009549313
- Address
- 24981 Palmilla Dr, Calabasas, CA, 91302
Frequently asked questions
How many devices does ALWAYS MORE MARKETING INC have in the registry?
The registry currently lists 4 devices for ALWAYS MORE MARKETING INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list ALWAYS MORE MARKETING INC's devices?
Among its 4 most recently registered devices, ALWAYS MORE MARKETING INC has devices listed in FDA 510(k) (4 devices).
What risk classes do ALWAYS MORE MARKETING INC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for ALWAYS MORE MARKETING INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ALWAYS MORE MARKETING INC in the registry?
The most recently registered devices listed for ALWAYS MORE MARKETING INC include DR GREENBURGS HYBRID ACRYLIC, Zyppah Anti-Snoring Device, DR GREENBURGS HYBRID VACUUM and DR. GREENSBURG'S HYBRID.