Data / Medical devices / Neuromuscular Tongue Muscle Stimulator For The Reduction Of Snoring And Obstructive Sleep Apnea
Neuromuscular Tongue Muscle Stimulator For The Reduction Of Snoring And Obstructive Sleep Apnea (QNO): 4 FDA-registered makers in 4 countries
4 establishments in 4 countries are registered with the FDA to make Neuromuscular Tongue Muscle Stimulator For The Reduction Of Snoring And Obstructive Sleep Apnea (product code QNO, Class 2, 21 CFR 872.5575). 1 of them has a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on May 16, 2024, and lists 0 recall events (0 Class I). FDA data exported November 3, 2026.
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- Product code
- QNO
- Device class
- 2
- Regulation
- 872.5575
- Medical specialty
- Dental
Makers by country
| Country | Makers |
|---|---|
| United Kingdom | 1 |
| Germany | 1 |
| China | 1 |
| Mexico | 1 |
Makers of Neuromuscular Tongue Muscle Stimulator For The Reduction Of Snoring And Obstructive Sleep Apnea
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Signifier Medical Technologies Limited | Manchester, United Kingdom | Manufacturer | 3 | May 16, 2024 | 0 | 0 | 0 | api.fda.gov |
| Freudenberg Medical Europe GMBH | Kaiserslautern Rhineland-Palatinate, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Milli-Henry Electronics Co., Ltd. | Dongguan Guangdong, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Seacomp Displays | Tijuana Baja California, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated May 16, 2024. 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.