Manufacturer registered with FDA
Freudenberg Medical Europe GmbH
Kaiserslautern, Germany. Lists 1 dental device type with FDA across 1 registered establishment.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 0as applicant
- Markets registered in
- 1United States
- Establishments
- 1Germany
Devices listed with FDA
What Freudenberg Medical Europe GmbH currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Neuromuscular Tongue Muscle Stimulator for the Reduction of Snoring and Obstructive Sleep ApneaQNO · Class 2 | — | Maker | eXciteOSA | 2025 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| FREUDENBERG MEDICAL EUROPE GMBHFDA reg. 3013445086 | Kaiserslautern Rhineland-Palatinate, Germany | Contract manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10093787). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.