Apinator
Device, Anti-snoring
Allen J. Moses, DDS LTD
The following data is part of a premarket notification filed by Allen J. Moses, Dds Ltd with the FDA for Apinator.
Pre-market Notification Details
| Device ID | K160123 |
| 510k Number | K160123 |
| Device Name: | Apinator |
| Classification | Device, Anti-snoring |
| Applicant | Allen J. Moses, DDS LTD 233 S. Wacker Drive Chicago, IL 60606 |
| Contact | Allen J Moses |
| Correspondent | Gloria Pacini Allen J. Moses, DDS LTD 233 S. Wacker Drive Chicago, IL 60606 |
| Product Code | LRK |
| CFR Regulation Number | 872.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-01-20 |
| Decision Date | 2016-07-12 |
| Summary: | summary |
Trademark Results [Apinator]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 APINATOR 86271539 not registered Dead/Abandoned |
Moses, Allen J 2014-05-05 |
 APINATOR 86134662 not registered Dead/Abandoned |
Moses, Allen J 2013-12-04 |
 APINATOR 85387133 not registered Dead/Abandoned |
Moses, Allen J. 2011-08-02 |
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