Not currently registered with FDA under this name
General Electric Co.
Mchenry, IL, United States. Named as applicant on 5 dental 510(k) clearances between 1977 and 1981. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51977–1981
- Markets registered in
- 21 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1976–2026
Registered in 2 markets
Where regulators' registries name General Electric Co. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | General Electric Co. | 5 clearances | 1977–1981 | Below |
| Taiwan | TFDA | Manufacturer | GENERAL ELECTRIC COMPANY | 1 | 2004–2004 | 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
510(k) clearances
Clearances on which FDA names General Electric Co. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 9 Jun 1981 | K811103 | GE 900 | EHD Extraoral with Timer X-Ray Unit |
| 16 Jan 1980 | K792581 | GENERAL ELECTRIC PANELIPSE LD | EHD Extraoral with Timer X-Ray Unit |
| 4 Dec 1978 | K781630 | GE-700 INTRA ORAL X-RAY SYSTEM | EAP Intraoral X-Ray Unit |
| 22 Dec 1977 | K772184 | X-RAY SYSTEM FOR DENTAL APPLICATION | EAP Intraoral X-Ray Unit |
| 28 Sep 1977 | K771748 | INTRA ORAL X-RAY CONES | EAH Lead-Lined Radiographic Cone |
Sources
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 of the most recent filing, which can be a US agent.