Manufacturer registered with FDA
Envoy Medical Corporation
White Bear Lake, MN, United States. Lists 1 dental device type with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 1
- Brands and models
- 1
- 510(k) clearances
- 12008–2008
- Markets registered in
- 215 registrations outside the US
- Establishments
- 1United States
510(k) clearances per year, 2000–2026
Registered in 2 markets
Where regulators' registries name Envoy Medical Corporation as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Envoy Medical Corporation | 1 clearances | 2008–2008 | Below |
| Canada | Health Canada | Registration holder | ENVOY MEDICAL CORPORATION | 15 | 2008–2008 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What Envoy Medical Corporation currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Nose and Throat Ear CementNEA · Class 2 | — | Maker | EnvoyCem | 2008 |
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 |
|---|---|---|
| ENVOY MEDICAL CORPORATIONFDA reg. 3004007782 | White Bear Lake, MN, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9092560). 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.