Not currently registered with FDA under this name
Panoramic Corp.
Ft. Wayne, IN, United States. Named as applicant on 6 dental 510(k) clearances between 1987 and 2016. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 61987–2016
- Markets registered in
- 21 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1980–2026
Registered in 2 markets
Where regulators' registries name Panoramic Corp. 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 | Panoramic Corp. | 6 clearances | 1987–2016 | Below |
| South Korea | MFDS | Manufacturer | Panoramic Corporation | 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 Panoramic Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 4 Feb 2016 | K152489 | ENCOMPASS Eagle 3D CBCT/Panoramic/Cephalometric Dental X-Ray | OAS Dental Computed Tomography X-Ray |
| 30 Jul 2014 | K141130 | ENCOMPASS | MUH Digital Extraoral Source X-Ray System |
| 17 Mar 2011 | K110371 | ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAY | MUH Digital Extraoral Source X-Ray System |
| 13 Jan 2005 | K043557 | MODEL PC-1000 PANORAMIC/CEPHALOMETRIC X-RAY SYSTEMS | EHD Extraoral with Timer X-Ray Unit |
| 4 Aug 1988 | K882436 | LASER - 1000 | EHD Extraoral with Timer X-Ray Unit |
| 13 Feb 1987 | K870236 | PANORAMIC X-RAY MODEL PC-1000 | EHD Extraoral with Timer X-Ray Unit |
Some of these clearances are listed with FDA today by another company: Young Innovations Inc (6).
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.