Not currently registered with FDA under this name
Porex Surgical, Inc.
Newnan, GA, United States. Named as applicant on 3 dental 510(k) clearances between 2010 and 2011. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 32010–2011
- Markets registered in
- 21 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 2007–2026
Registered in 2 markets
Where regulators' registries name Porex Surgical, Inc. 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 | Porex Surgical, Inc. | 3 clearances | 2010–2011 | Below |
| South Korea | MFDS | Manufacturer | Porex Surgical, Inc. | 1 | 2009–2009 | 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 Porex Surgical, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 7 Jan 2011 | K102184 | MEDPOR CONTAIN CAN IMPLANT | NPK Intraoral Synthetic Barrier |
| 28 Jun 2010 | K091807 | MEDPOR FIXATION SYSTEM | JEY Bone Plate |
| 19 Mar 2010 | K091120 | MEDPOR CONTAIN IMPLANT | NPK Intraoral Synthetic Barrier |
Some of these clearances are listed with FDA today by another company: Stryker (2).
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.